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AirWrap

FDA UDI

Class I (US FDA UDI)

by Revmedx, Inc.

Identity

Trade Name
AirWrap FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
Pressure bandage FDA UDI
Model / Reference
FIN-0005-01 FDA UDI
Description
Pressure bandage FDA UDI

Identifiers

Catalog Number
FIN-0005-01 FDA UDI
Primary DI / UDI-DI
00851587006080 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
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

Dimensions & Sizes

Size
Width — 4 Inch FDA UDI

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

AirWrap by Revmedx, Inc. — 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
Revmedx, Inc.

Sources (1)

  • FDA UDI 3c9bdeae-9965-43e3-9af0-f5915b19987a 37 fields · synced May 31, 2026