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Transradial Pressure Bandage

FDA UDI

Class I (US FDA UDI)

by Valflux Group, Llc

Identity

Trade Name
TRANSRADIAL PRESSURE BANDAGE FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
VGPB04B TRANSRADIAL PRESSURE BANDAGE FDA UDI
Model / Reference
VGPB04B FDA UDI
Description
VGPB04B TRANSRADIAL PRESSURE BANDAGE FDA UDI

Identifiers

Catalog Number
VGPB04B FDA UDI
Primary DI / UDI-DI
00850004162255 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Transradial Pressure Bandage by Valflux Group, Llc — 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
Valflux Group, Llc

Sources (1)

  • FDA UDI 0df92036-283b-40f9-a017-99832c1af513 35 fields · synced Jun 8, 2026