AccessGUDID - DEVICE: VERIFY (10724995002319)

GUDID

Device Identifier (DI) Information

Brand Name: VERIFY
Version or Model: Resi-Test
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 2D73QH
Company Name: STERIS CORPORATION

Primary DI Number: 10724995002319
Issuing Agency: GS1
Commercial Distribution End Date: May 23, 2022
Device Count: 25
Labeler D-U-N-S® Number*: 961394798 *Terms of Use

Device Description: Brush for VERIFY RESI-TEST SLIDE-THRU Cleaning Indicator, Small is designed to detect a broad spectrum of protein residues and is intended for use after manual or automated cleaning and prior to high level disinfection or sterilization.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
38835	Surgical instrument/endoscope cleaning utensil, single-use	A non-absorbent, non-powered, hand-held device in the form of a brush, a wire, strip of metal, or handle intended to clean the exterior and/or interior (lumen) of a surgical instrument (e.g., bur, reamer, bone tap, suturing device, sheath/shaft, ultrasonic surgical handpiece) and/or endoscope. The bristles, fibres or spines of brushes may be mounted along a single plane or radiate out around a central shaft, and may be soft or stiff; the shaft/handle of brushes may be flexible or rigid. The device may be used to clean endoscopic or open-surgery instruments, and it may have a handle or a connector/adaptor at the proximal end. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MNL	ACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 6b6aed50-ce0e-4b24-8708-2538fe9f4e5e
Public Version Date: June 10, 2022
Public Version Number: 3
DI Record Publish Date: March 31, 2021