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Battle Bandage

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
BATTLE BANDAGE FDA UDI
Generic Name
Wound dressing kit, non-medicated FDA UDI
Device Name
Battle Bandage 1 ea. - 8" x 8", sterile gauze pad with 6' x 4", clear, self adhering, compression wrap FDA UDI
Model / Reference
06 FDA UDI
Description
Battle Bandage 1 ea. - 8" x 8", sterile gauze pad with 6' x 4", clear, self adhering, compression wrap FDA UDI

Identifiers

Catalog Number
32-700 FDA UDI
Primary DI / UDI-DI
M68932700060 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Wound dressing kit, non-medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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: Wound dressing kit, non-medicated

Battle Bandage by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound dressing kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2da08da0-f0aa-4fc1-b8f9-d75966f69e16 35 fields · synced Jun 1, 2026