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Battle Wrap

FDA UDI

Class I (US FDA UDI)

by Safeguard Us Operating, Llc

Identity

Trade Name
Battle Wrap FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
1ea. - 6' x 4", clear, self-adhering, compression wrap FDA UDI
Model / Reference
5 FDA UDI
Description
1ea. - 6' x 4", clear, self-adhering, compression wrap FDA UDI

Identifiers

Catalog Number
02-001 FDA UDI
Primary DI / UDI-DI
M68902001050 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use 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

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

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

Battle Wrap 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

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Manufacturer

Sources (1)

  • FDA UDI ff4b5fb6-3d53-4ff4-8464-c44609ebc93f 36 fields · synced Jun 8, 2026