Last synced on 9 May 2025 at 11:05 pm

Rigid Sterilization Container With Software

Page Type
Product Code
Definition
The rigid sterilization container with software is intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. It is intended to allow sterilization of the enclosed medical device(s) and to maintain sterility until used. The rigid sterilization container with software is designed for use with high-vacuum or pulse-vacuum steam sterilization systems.
Physical State
Rigid sterilization container comprised of metal and polymers that contains software that controls valves and monitors sterilization cycle status.
Technical Method
Used with steam sterilizers to allow sterilization and maintain sterility of devices undergoing steam sterilization
Target Area
Does not contact the patient.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6855
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QJT is linked to regulation 21CFR880.6855, which does not seem to exist yet. It may be pending at the moment.

Rigid Sterilization Container With Software

Page Type
Product Code
Definition
The rigid sterilization container with software is intended to be used to enclose another medical device that is to be sterilized by a healthcare provider. It is intended to allow sterilization of the enclosed medical device(s) and to maintain sterility until used. The rigid sterilization container with software is designed for use with high-vacuum or pulse-vacuum steam sterilization systems.
Physical State
Rigid sterilization container comprised of metal and polymers that contains software that controls valves and monitors sterilization cycle status.
Technical Method
Used with steam sterilizers to allow sterilization and maintain sterility of devices undergoing steam sterilization
Target Area
Does not contact the patient.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6855
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QJT is linked to regulation 21CFR880.6855, which does not seem to exist yet. It may be pending at the moment.