K093493 · Aesculap, Inc. · FRG · Jul 27, 2010 · General Hospital
Device Facts
Record ID
K093493
Device Name
AESCULAP STERILCONTAINER S
Applicant
Aesculap, Inc.
Product Code
FRG · General Hospital
Decision Date
Jul 27, 2010
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 880.6850
Device Class
Class 2
Indications for Use
The Aesculap Sterilcontainer S is a reusable sterilization container system (consisting of perforated bottoms and perforated lids with filter retention plates, and disposable polypropylene filters) intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. This container has been validated with stainless steel lumens, hinged, and knurled instruments. It is intended to allow sterilization of the enclosed device and also maintain sterility of the enclosed device until used. This container system is compatible for use with the STERRAD 200, STERRAD NX (Standard cycle and Advanced cycle), and STERRAD 100NX (Standard cycle and Flex cycle). The Sterilcontainer S System includes accessories such as silicone mats, baskets, trays, racks, eyepiece holders and sleeve holders.
Device Story
Reusable sterilization container system; non-anodized aluminum construction; utilizes disposable polypropylene filters. Designed to enclose medical devices during sterilization and maintain sterility during storage. Used by healthcare providers in clinical settings. Compatible with STERRAD 200, STERRAD NX, and STERRAD 100NX hydrogen peroxide gas plasma sterilization systems. Accessories include silicone mats, baskets, trays, racks, eyepiece holders, and sleeve holders. Validated for various stainless steel lumen sizes and configurations. Protects instruments from contamination post-sterilization; ensures sterility maintenance for up to 30 days.
Clinical Evidence
Bench testing only. Validation conducted in accordance with FDA guidance and AAMI standards. Testing confirmed sterilization efficacy and sterility maintenance for 30 days across specified STERRAD cycles (200, NX, 100NX) for various stainless steel and PTFE/PE lumen configurations.
Technological Characteristics
Non-anodized aluminum container; disposable polypropylene filter; perforated lid and bottom with filter retention plates. Dimensions vary by size (Full, 3/4, 1/2, 1/4, Extra Long Mini). Accessories include silicone mats, baskets, trays, racks. No software or electronic components.
Indications for Use
Indicated for healthcare providers to enclose and sterilize medical devices, including stainless steel lumens, hinged, and knurled instruments. Compatible with STERRAD 200, STERRAD NX (Standard/Advanced cycles), and STERRAD 100NX (Standard/Flex cycles). Specific lumen requirements: STERRAD 200 (≥3mm ID x ≤400mm L), STERRAD NX Standard (≥2mm ID x ≤400mm L), STERRAD NX Advanced (≥1mm ID x ≤500mm L), STERRAD 100NX Standard (≥0.7mm ID x ≤500mm L), STERRAD 100NX Flex (porous flexible endoscope ≥1mm ID x ≤850mm L).
Regulatory Classification
Identification
A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.
SteriTite Universal Container System with MediTray Products for STERRAD 200, STERRAD NX, Ozone 125L, Sterilization, and Prevacuum Steam Flash Sterilization (K080558)
Submission Summary (Full Text)
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KCA343
Page 1 of 5
| B. | 510(k) SUMMARY (as required by 21 CFR 807.92) | |
|----------------------|--------------------------------------------------------------------------------------------------------------------|--------------|
| | Aesculap Sterilcontainer S for<br>STERRAD 200, STERRAD NX, and STERRAD NX100<br>July 27, 2010 | |
| COMPANY: | Aesculap®, Inc.<br>3773 Corporate Parkway<br>Center Valley, PA 18034<br>Establishment Registration Number: 2916714 | JUL 2-7 2010 |
| CONTACT: | Kathy A. Racosky<br>610-984-9291 (phone)<br>610-791-6882 (fax) | |
| TRADE NAME: | Aesculap Sterilcontainer 'S | |
| COMMON NAME: | Sterilization Container Wrap | |
| CLASSIFICATION NAME: | Wrap, Sterilization | |
| REGULATION NUMBER: | 880.6850 | |
| PRODUCT CODE: | FRG | |
### SUBSTANTIAL EQUIVALENCE
Aesculap®, Inc. believes that the SterilContainer S is substantially equivalent to:
- Aesculap STERRAD 100S Compatible Sterilcontainer (K040865), .
- SteriTite Universal Container System with MediTray Products for STERRAD 200, . STERRAD NX, Ozone 125L, Sterilization, and Prevacuum Steam Flash Sterilization (K080558).
## DEVICE DESCRIPTION
The Aesculap Sterilcontainer S is designed as a container system that will allow for sterilization and storage of other medical devices. This container is designed to be compatible for use with the STERRAD sterilization processes [200, NX (Standard cycle and Advanced cycle), and 100NX (Standard cycle and Flex cycle). The container is made from non-anodized Aluminum and utilizes a disposable (single use) polypropylene filter. The Sterilcontainer S System includes accessories such as silicone mats, baskets, trays, racks, eyepiece holders and sleeve holders.
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### INDICATIONS FOR USE:
The Aesculap Sterilcontainer S is a reusable sterilization container system (consisting of perforated bottoms and perforated lids with filter retention plates, and disposable polypropylene filters) intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. This container has been validated with stainless steel lumens, hinged, and knurled instruments. It is intended to allow sterilization of the enclosed device and also maintain sterility of the enclosed device until used. This container system is compatible for use with the STERRAD 200, STERRAD NX (Standard cycle and Advanced cycle), and STERRAD 100NX (Standard cycle and Flex cycle). The Sterilcontainer S System includes accessories such as silicone mats, baskets, trays, racks, eyepiece holders and sleeve holders.
The Sterilcontainer S is recommended for surface and lumens:
STERRAD 200, stainless steel lumens ≥ 3mm I.D. x ≤ 400mm L STERRAD NX standard cycle, stainless steel lumens ≥ 2mm I.D. x ≤ 400mm L STERRAD NX advanced cycle, stainless steel lumens ≥ 1mm I.D. x ≤ 500mm L STERRAD 100NX standard cycle, stainless steel lumens ≥ 0.7mm I.D. x ≤ 500mm L STERRAD 100NX flex cycle, porous lumens (flexible endoscope) ≥ 1mm I.D. x ≤ 850mm L
30 days of shelf life testing has been conducted for the Sterilicontainer S.
The attached tables identify which products may be sterilized in which STERRAD sterilization cycle.
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Page 3 of 5
| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|-------------------|--------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ¼") | 21.46 |
| JM441 | Full Size Perforated Bottom 120mm (5 ½") | 21.46 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 21.46 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 21.46 |
| JM740 | ¾ Size Perforated Bottom 90mm(4 ¼") | 14.42 |
| JM741 | ¾ Size Perforated Bottom 120mm (5 ½") | 14.42 |
| JM742 | ¾ Size Perforated Bottom 135mm (6") | 14.42 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 14.42 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 14.42 |
| JM342 | ½ Size Perforated Bottom 135mm (6") | 14.42 |
| JM344 | ½ Size Perforated Bottom 187mm (8") | 14.42 |
| JM094 | ¼ Size Perforated Bottom with Lid 65mm (2 ½") | 14.42 |
| JM096 | ¼ Size Perforated Bottom with Lid 130mm (5 1/8") | 14.42 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | ¾ Size Lid | |
| JM389 | ½ Size Lid | |
| See JM094 & JM096 | ¼ Size Lid | |
| JM020 | Extra Long Mini Lid | |
TABLE 1 ilContainer & Comp tible Containers in STERBAD 200
Note: Full, ¾, ½, and ¼ size containers have been validated with 5 stainless steel lumens per container system. The Extra Long Mini container has been validated with 2 stainless steel lumens per container system.
## TABLE 2 SterilContainer S Compatible Containers in STERRAD NX Standard and Advanced Cvcle
| Item # | Description | Total loaded<br>container weight<br>(lbs) |
|-------------------|--------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ¼") | 21.46 |
| JM441 | Full Size Perforated Bottom 120mm (5 ½") | 21.46 |
| JM740 | ¾ Size Perforated Bottom 90mm (4 ¼") | 13.85 |
| JM741 | ¾ Size Perforated Bottom 120mm (5 ½") | 13.85 |
| JM742 | ¾ Size Perforated Bottom 135mm (6") | 13.85 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 13.85 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 13.85 |
| JM094 | ¼ Size Perforated Bottom with Lid 65mm (2 ½") | 13.85 |
| JM096 | ½ Size Perforated Bottom with Lid 130mm (5 1/8") | 13.85 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | 3/4 Size Lid | |
| JM389 | ½ Size Lid | |
| See JM094 & JM096 | ¼ Size Lid | |
| JM020 | Extra Long Mini Lid | |
Note: Full, ¾, ½, and ¼ size containers have been validated with 5 stainless steel lumens per container system. The Extra Long Mini container has been validated with 2 stainless steel lumens per container system.
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| TABLE 3 |
|----------------------------------------------------------|
| SterilContainer S Compatible Containers in STERRAD 100NX |
| Standard Cycle |
.
| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|-------------------|--------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ¼") | 21.46 |
| JM441 | Full Size Perforated Bottom 120mm (5 ½") | 21.46 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 21.46 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 21.46 |
| JM740 | ¾ Size Perforated Bottom 90mm(4 ¼") | 13.85 |
| JM741 | ¾ Size Perforated Bottom 120mm (5 ½") | 13.85 |
| JM742 | ¾ Size Perforated Bottom 135mm (6") | 13.85 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 13.85 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 13.85 |
| JM342 | ½ Size Perforated Bottom 135mm (6") | 13.85 |
| JM344 | ½ Size Perforated Bottom 187mm (8") | 13.85 |
| JM094 | ¼ Size Perforated Bottom with Lid 65mm (2 ½") | 13.85 |
| JM096 | ¼ Size Perforated Bottom with Lid 130mm (5 1/8") | 13.85 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | ¾ Size Lid | |
| JM389 | ½ Size Lid | |
| See JM094 & JM096 | ¼ Size Lid | |
| JM020 | Extra Long Mini Lid | |
Note: Full, ¾, ½, and ¼ size containers have been validated with 5 stainless steel lumens per container system. The Extra Long Mini container has been validated with 2 stainless steel lumens per container system.
## TABLE 4 SterilContainer S Compatible Containers in STERRAD 100NX Flex Cycle
| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|--------|------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ¼") | 9.67 |
| JM441 | Full Size Perforated Bottom 120mm (5 ½") | 9.67 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 9.67 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 9.67 |
| JM740 | ¾ Size Perforated Bottom 90mm(4 ¼") | 9.67 |
| JM741 | ¾ Size Perforated Bottom 120mm (5 ½") | 9.67 |
| JM742 | ¾ Size Perforated Bottom 135mm (6") | 9.67 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 9.67 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 9.67 |
| JM342 | ½ Size Perforated Bottom 135mm (6") | 9.67 |
| JM344 | ½ Size Perforated Bottom 187mm (8") | 9.67 |
| JM489 | Full Size Lid | |
| JM789 | ¾ Size Lid | |
| JM389 | ½ Size Lid | |
Note: Full, ¾, and ½ size containers have been validated with 1 PTFE/PE lumen per container system.
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## TECHNOLIGICAL CHARACTERISTICS(compared to predicate(s)}
The Aesculap Sterilcontainer S is compatible for use in STERRAD 200, STERRAD NX (Standard cycle and Advanced cycle), and STERRAD 100NX (Standard cycle and Flex cycle). The Sterilcontainer is offered in similar shapes and sizes as the predicate devices. The material used for the STERRAD Compatible Aesculap Sterilcontainer S is the same as that used to manufacture the predicate devices.
## PERFORMANCE DATA
All required testing per "Draft Guidance for the Preparation of Premarket Notifications 510(k)'s" for Aesculap Sterilcontainer S was completed. The Aesculap Sterilcontainer S was fully validated for STERRAD 200, STERRAD NX (Standard cycle and Advanced cycle), and STERRAD 100NX (Standard cycle and Flex cycle). Sterilization Systems. This validation was conducted in accordance with FDA guidance and available AAMI standards by a qualified testing laboratory.
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# DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/5/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized emblem resembling a caduceus, with three wave-like lines representing the department's mission of promoting health and well-being. The emblem is accompanied by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular fashion around the emblem.
#### Public Health Service
Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Ms. Kathy Racosky Regulatory Affairs Specialist AESCULAP, Incorporated 3773 Corporate Parkway Center Valley, Pennsylvania 18034
Re: K093493
Trade/Device Name: AESCULAP Sterilcontainer S Regulation Number: 21 CFR 880.6850 Regulation Name: Sterilization Wrap Regulatory Class: II Product Code: FRG Dated: June 29, 2010 Received: June 30, 2010
JUL 2-7 2010
Dear Ms. Racosky:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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### Page 2- Ms. Racosky
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801). please go to
http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.
Sincerely yours,
Susan Luong
Anthony D. Watson, B.S., M.S., M.B.A. Director
Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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### INDICATIONS FOR USE STATEMENT
JUL 27 2010
K093493
510(k) Number:
## Device Name: Aesculap Sterilcontainer S
### Indications for Use:
The Aesculap Sterilcontainer S is a reusable sterilization container system (consisting of perforated bottoms and perforated lids with filter retention plates, and disposable polypropylene filters) intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. This confainer has been validated with stainless steel lumens, hinged, and knurled instruments. It is intended to allow sterilization of the enclosed device and also maintain sterility of the enclosed device until used. This container system is compatible for use with the STERRAD 200, STERRAD NX (Standard cycle and Advanced cycle), and STERRAD 100NX (Standard cycle and Flex cycle). The Steriicontainer S System includes accessories such as silicone mats, baskets, trays, racks, eyepiece holders and sleeve holders.
The Stericontainer S is recommended for surface and lumens:
STERRAD 200, stainless steel lumens ≥ 3mm I.D. x ≤ 400mm L STERRAD NX standard cycle, stainless steel lumens ≥ 2mm 1.D. x ≤ 400mm L STERRAD NX advanced cycle, stainless steel lumens ≥ 1mm 1.D. x ≤ 500mm L STERRAD 100NX standard cycle, stainless steel lumens ≥ 0.7mm |.D. x ≤ 500mm L STERRAD 100NX flex cycle, porous lumens (flexible endoscope) ≥ 1mm I.D. x ≤ 850mm L
30 days of shelf life testing has been conducted for the Sterilicontainer S.
The attached tables identify which products may be sterilized in which STERRAD sterilization cycle.
Prescription Use
and/or . Over-the-Counter Use __
(per 21 CFR 801 Subpart D)
(per 21 CFR 801 Subpart C)
PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE)
Page 1 of 3
(Division Sign-Uff) (Division Sign-On)
Division of Anesthesiology, General Hospital
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| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|-------------------|--------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ¼") | 21.46 |
| JM441 | Full Size Perforated Bottom 120mm (5 ½") | 21.46 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 21.46 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 21.46 |
| JM740 | ¾ Size Perforated Bottom 90mm(4 ¼") | 14.42 |
| JM741 | ¾ Size Perforated Bottom 120mm (5 ½") | 14.42 |
| JM742 | ¾ Size Perforated Bottom 135mm (6") | 14.42 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 14.42 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 14.42 |
| JM342 | ½ Size Perforated Bottom 135mm (6") | 14.42 |
| JM344 | ½ Size Perforated Bottom 187mm (8") | 14.42 |
| JM094 | ¼ Size Perforated Bottom with Lid 65mm (2 ½") | 14.42 |
| JM096 | ¼ Size Perforated Bottom with Lid 130mm (5 1/8") | 14.42 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | ¾ Size Lid | |
| JM389 | ½ Size Lid | |
| See JM094 & JM096 | ¼ Size Lid | |
| JM020 | Extra Long Mini Lid | |
TABLE 1 SterilContainer S Compatible Containers in STERRAD 200
Note: Full, ¾, ½, and ¼ size containers have been validated with 5 stainless steel lumens per container system. The Extra Long Mini container has been validated with 2 stainless steel lumens per container system.
## TABLE 2 SterilContainer S Compatible Containers in STERRAD NX Standard and Advanced Cycle
| Item # | Description | Total loaded<br>container weight<br>(lbs) |
|-------------------|----------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 1/4") | 21,46 |
| JM441 | Full Size Perforated Bottom 120mm (5 1/2") | 21.46 |
| JM740 | 3/4 Size Perforated Bottom 90mm (4 1/4") | 13.85 |
| JM741 | 3/4 Size Perforated Bottom 120mm (5 1/2") | 13.85 |
| JM742 | 3/4 Size Perforated Bottom 135mm (6") | 13.85 |
| JM340 | 1/2 Size Perforated Bottom 90mm (4 1/4") | 13.85 |
| JM341 | 1/2 Size Perforated Bottom 120mm (5 1/2") | 13.85 |
| JM094 | 1/4 Size Perforated Bottom with Lid 65mm (2 1/2") | 13.85 |
| JM096 | 1/4 Size Perforated Bottom with Lid 130mm (5 1/8") | 13.85 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | 3/4 Size Lid | |
| JM389 | ½ Size Lid | |
| See JM094 & JM096 | 1/4 Size Lid | |
| JM020 | Extra Long Mini Lid | |
Note: Full, ¼, ½, and ¼ size containers have been validated with 5 stainless steel lumens per container system. The Extra Long Mini container has been validated with 2 stainless steel lumens per container system.
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## TABLE 3 SterilContainer S Compatible Containers in STERRAD 100NX Standard Cycle
| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|-------------------|----------------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 1/4") | 21.46 |
| JM441 | Full Size Perforated Bottom 120mm (5 1/2") | 21.46 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 21.46 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 21.46 |
| JM740 | 3/4 Size Perforated Bottom 90mm(4 1/4") | 13.85 |
| JM741 | 3/4 Size Perforated Bottom 120mm (5 1/2") | 13.85 |
| JM742 | 3/4 Size Perforated Bottom 135mm (6") | 13.85 |
| JM340 | 1/2 Size Perforated Bottom 90mm (4 1/4") | 13.85 |
| JM341 | 1/2 Size Perforated Bottom 120mm (5 1/2") | 13.85 |
| JM342 | 1/2 Size Perforated Bottom 135mm (6") | 13.85 |
| JM344 | 1/2 Size Perforated Bottom 187mm (8") | 13.85 |
| JM094 | 1/4 Size Perforated Bottom with Lid 65mm (2 1/2") | 13.85 |
| JM096 | 1/4 Size Perforated Bottom with Lid 130mm (5 1/8") | 13.85 |
| JM021 | Extra Long Mini Bottom 73mm (3") | 7.64 |
| JM489 | Full Size Lid | |
| JM789 | 3/4 Size Lid | |
| JM389 | 1/2 Size Lid | |
| See JM094 & JM096 | 1/4 Size Lid | |
| JM020 | Extra Long Mini Lid | |
Note: Full, ¾, ½, and ¼ size containers have been validated with 5 stainless steel lumens per Note: I dir, %, 72, and 14 oize oonlainer has been validated with 2 stainless steel lumens per container system.
## TABLE 4 SterilContainer S Compatible Containers in STERRAD 100NX Flex Cycle
| Item # | Description | Total loaded<br>container<br>weight (lbs) |
|--------|--------------------------------------------|-------------------------------------------|
| JM440 | Full Size Perforated Bottom 90mm (4 ½") | 9.67 |
| JM441 | Full Size Perforated Bottom 120mm (5 1/2") | 9.67 |
| JM442 | Full Size Perforated Bottom 135mm (6") | 9.67 |
| JM444 | Full Size Perforated Bottom 187mm (8") | 9.67 |
| JM740 | 3/4 Size Perforated Bottom 90mm(4 ½") | 9.67 |
| JM741 | 3/4 Size Perforated Bottom 120mm (5 1/2") | 9.67 |
| JM742 | 3/4 Size Perforated Bottom 135mm (6") | 9.67 |
| JM340 | ½ Size Perforated Bottom 90mm (4 ¼") | 9.67 |
| JM341 | ½ Size Perforated Bottom 120mm (5 ½") | 9.67 |
| JM342 | ½ Size Perforated Bottom 135mm (6") | 9.67 |
| JM344 | ½ Size Perforated Bottom 187mm (8") | 9.67 |
| JM489 | Full Size Lid. | |
| JM789 | 3/4 Size Lid | |
| JM389 | ½ Size Lid | |
Note: Full, ¾, and ½ size containers have been validated with 1 PTFE/PE lumen per container system.
Page 3 ol 3
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.