AccessGUDID - DEVICE: TipStop (07332414113858)

GUDID

Device Identifier (DI) Information

Brand Name: TipStop
Version or Model: 114555
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 114555
Company Name: BAXTER HEALTHCARE CORPORATION

Primary DI Number: 07332414113858
Issuing Agency: GS1
Commercial Distribution End Date: June 22, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 005083209 *Terms of Use

Device Description: TipStop is a compressive dressing made of a polyamide compressive element covered with alginate, placed on adhesive film. TipStop has been specially designed to stop bleeding after venipuncture. TipStop is sterilised by irradiation. This product is not made with natural rubber latex.

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):	Yes
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?
10284	Pressure bandage, non-latex, single-use	A strip or roll of fabric or plastic material (non-natural rubber latex) intended to be applied to and compress a local area of the body for one or more preventative/therapeutic applications (e.g., prevent oedema, support injuries associated with minor trauma, treat disorders of venous return). It may be described as a sports tape intended for support while allowing movement, or described as a compression bandage; it is not intended to be used in association with open wounds. It is intended for use in the home or healthcare facility. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KMF	Bandage, liquid

FDA Premarket Submission

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

Device Exempt from Premarket Submission: No 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
Storage Environment Temperature: between 0 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 7ab4fcfe-e8a3-47af-b9de-69b7f7d8566c
Public Version Date: August 25, 2023
Public Version Number: 3
DI Record Publish Date: February 01, 2019