Last synced on 9 May 2025 at 11:05 pm

Qualitative Cleaning Process Protein Indicator

Page Type
Product Code
Definition
A qualitative cleaning process protein indicator is intended for use by a health care provider on a cleaned medical device as an interim step prior to high level disinfection or sterilization of the cleaned medical device. The intended use is to inform the health care user of the presence of residual soil protein in the sample extract.
Physical State
Protein detection indicator designed for use in the reprocessing of medical devices in health care settings. The device may include additional components for sampling. The device may include a color chart for qualitative indication of the residual soil protein.
Technical Method
A physical or chemical change occurs at the presence of the residual protein at levels relevant to cleaning validation endpoints.
Target Area
The device is intended to be used on a cleaned medical device prior to high level disinfection or sterilization of the cleaned medical device.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6930
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 SDC is linked to regulation 21CFR880.6930, which does not seem to exist yet. It may be pending at the moment.

Qualitative Cleaning Process Protein Indicator

Page Type
Product Code
Definition
A qualitative cleaning process protein indicator is intended for use by a health care provider on a cleaned medical device as an interim step prior to high level disinfection or sterilization of the cleaned medical device. The intended use is to inform the health care user of the presence of residual soil protein in the sample extract.
Physical State
Protein detection indicator designed for use in the reprocessing of medical devices in health care settings. The device may include additional components for sampling. The device may include a color chart for qualitative indication of the residual soil protein.
Technical Method
A physical or chemical change occurs at the presence of the residual protein at levels relevant to cleaning validation endpoints.
Target Area
The device is intended to be used on a cleaned medical device prior to high level disinfection or sterilization of the cleaned medical device.
Regulation Medical Specialty
General Hospital
Review Panel
General Hospital
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
880.6930
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 SDC is linked to regulation 21CFR880.6930, which does not seem to exist yet. It may be pending at the moment.