← Back to catalogue

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
03 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
M68932700030 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
Not 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a6fa4521-a5e7-4f8a-b48a-22683e3bf1bc 35 fields · synced May 30, 2026