Last synced on 25 January 2026 at 3:41 am

Ultraviolet Light-Based Microbial Reduction Device For Luer-Activated Valves

Page Type
Product Code
Definition
An ultraviolet light-based microbial reduction device for luer-activated valves is a device that uses ultraviolet light to irradiate luer-activated valves (e.g., as used for intravascular administration). The device is intended to supplement the manual, physical microbicidal treatment of luer-activated valves by providing limited microbial reduction, and is not intended to disinfect or replace manual microbicidal treatment.
Physical State
The device consists of a handheld lamp unit and disposable barrier caps.
Technical Method
The device uses an ultraviolet lamp to reduce the microbial population after manual disinfection.
Target Area
Needleless connectors for peripherally-inserted central catheter (PICC) lines.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6512
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 SGX is linked to regulation 21CFR880.6512, which does not seem to exist yet. It may be pending at the moment.

Ultraviolet Light-Based Microbial Reduction Device For Luer-Activated Valves

Page Type
Product Code
Definition
An ultraviolet light-based microbial reduction device for luer-activated valves is a device that uses ultraviolet light to irradiate luer-activated valves (e.g., as used for intravascular administration). The device is intended to supplement the manual, physical microbicidal treatment of luer-activated valves by providing limited microbial reduction, and is not intended to disinfect or replace manual microbicidal treatment.
Physical State
The device consists of a handheld lamp unit and disposable barrier caps.
Technical Method
The device uses an ultraviolet lamp to reduce the microbial population after manual disinfection.
Target Area
Needleless connectors for peripherally-inserted central catheter (PICC) lines.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6512
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 SGX is linked to regulation 21CFR880.6512, which does not seem to exist yet. It may be pending at the moment.