Multi-Trauma Dressing

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Multi-Trauma Dressing FDA UDI
Generic Name: Pressure bandage, non-latex, single-use FDA UDI
Device Name: Multi-Trauma Dressing, Sterile, 12"x30" FDA UDI
Model / Reference: 3532 FDA UDI
Description: Multi-Trauma Dressing, Sterile, 12"x30" FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784353210 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

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

Multi-Trauma Dressing by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dynarex Corp.

Sources (1)

FDA UDI eeea7240-6ab6-41d1-a93b-4eca1e6718d0 33 fields · synced Jun 6, 2026