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TipStop

FDA UDI

Class I (US FDA UDI)

by Baxter Healthcare Corp

Identity

Trade Name
TipStop FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
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. FDA UDI
Model / Reference
114555 FDA UDI
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. FDA UDI

Identifiers

Catalog Number
114555 FDA UDI
Primary DI / UDI-DI
07332414113858 FDA UDI
FDA Product Code
KMF FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

TipStop by Baxter Healthcare Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Baxter Healthcare Corp

Sources (1)

  • FDA UDI 7ab4fcfe-e8a3-47af-b9de-69b7f7d8566c 37 fields · synced Jun 8, 2026