AccessGUDID - DEVICE: Q-Stop (00860011629405)

GUDID

Device Identifier (DI) Information

Brand Name: Q-Stop
Version or Model: QS
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: DRS Vascular, Inc.

Primary DI Number: 00860011629405
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 6
Labeler D-U-N-S® Number*: 119066556 *Terms of Use

Device Description: The device is designed to be placed temporarily over a skin incision to assist with holding suture tension prior to final closure.

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):	Yes
Over the Counter (OTC):	No
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?
33519	Suture retention device	A device designed to be placed on the surface of the skin and intended to aid wound healing by distributing suture tension over a larger area in the patient. It is typically in the form of a retention bridge, a surgical button, or a suture bolster through which the sutures are passed. The distribution of suture tension will help prevent the suture from cutting the skin. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KGS	Retention Device, Suture

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: Yes
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: f7e76947-84f4-472e-8413-c3780ff31f40
Public Version Date: May 31, 2024
Public Version Number: 1
DI Record Publish Date: May 23, 2024