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 in. FDA UDI
- Model / Reference
- A1749003 FDA UDI
- Description
- Air-activated, one-time use adhesive heat pad, 3.8 x 10.3 in. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00072959019747 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
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.
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- TopCare health — Topco Associates, LLC · Class I
- GCB Medical Supply — GCB MEDICAL LLC · Class I
- CVS Health — WOONSOCKET PRESCRIPTION CENTER, INCORPORATED · Class I
- Walgreens — WALGREEN CO. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Alva/Amco Pharmacal Companies, Inc.
Sources (1)
- FDA UDI 2112f1ca-24db-46c4-b0e1-56be1a232a82 34 fields · synced May 30, 2026