Last synced on 9 May 2025 at 11:05 pm

Ultraviolet Radiation Disinfection Chamber Device

Page Type
Product Code
Definition
An ultraviolet radiation disinfection chamber device is intended to disinfect patient contacting medical devices using UV radiation after the device has been cleaned. Disinfection of the medical device is achieved within an enclosed chamber through the exposure to UV radiation.
Physical State
Chambered UV-C disinfection device used to achieve high level disinfection (HLD) of surfaces of semi-critical transvaginal, semi-critical transrectal and external intact skin contacting ultrasound probes.
Technical Method
Microbial reduction on surfaces of medical devices using a UV-C germicidal device.
Target Area
External (intact skin contacting), Transvaginal and Transrectal ultrasound probes
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6511
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 SCS is linked to regulation 21CFR880.6511, which does not seem to exist yet. It may be pending at the moment.

Ultraviolet Radiation Disinfection Chamber Device

Page Type
Product Code
Definition
An ultraviolet radiation disinfection chamber device is intended to disinfect patient contacting medical devices using UV radiation after the device has been cleaned. Disinfection of the medical device is achieved within an enclosed chamber through the exposure to UV radiation.
Physical State
Chambered UV-C disinfection device used to achieve high level disinfection (HLD) of surfaces of semi-critical transvaginal, semi-critical transrectal and external intact skin contacting ultrasound probes.
Technical Method
Microbial reduction on surfaces of medical devices using a UV-C germicidal device.
Target Area
External (intact skin contacting), Transvaginal and Transrectal ultrasound probes
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6511
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 SCS is linked to regulation 21CFR880.6511, which does not seem to exist yet. It may be pending at the moment.