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BackAid

FDA UDI

Class I (US FDA UDI)

by Alva/Amco Pharmacal Companies, Inc.

Identity

Trade Name
BackAid FDA UDI
Generic Name
Exothermic heat therapy pack/patch FDA UDI
Device Name
Air-activated, one-time use adhesive heat pad, 3.8 x 10.3 inch FDA UDI
Model / Reference
A1740003 FDA UDI
Description
Air-activated, one-time use adhesive heat pad, 3.8 x 10.3 inch FDA UDI

Identifiers

Primary DI / UDI-DI
00072959015749 FDA UDI
FDA Product Code
OMW FDA UDI
GMDN Term
Exothermic heat therapy pack/patch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5710 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

Category: Exothermic heat therapy pack/patch

BackAid by Alva/Amco Pharmacal Companies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exothermic heat therapy pack/patch.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 430e9aa9-cfad-444f-a84b-a30172698667 34 fields · synced May 31, 2026