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TipStop

FDA UDI

Class I (US FDA UDI)

by Adhex Technologies

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
03760339170825 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pressure bandage, non-latex, single-use

TipStop by Adhex Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adhex Technologies

Sources (1)

  • FDA UDI aaf3bf18-1f96-40cd-bcae-3cace1a20e3d 35 fields · synced May 30, 2026