Identity
- Trade Name
- Beyond BodiHeat® FDA UDI
- Generic Name
- Hot/cold therapy pack, single-use FDA UDI
- Device Name
- Disposable heat pad for pain relief, non-medicated, apply over-clothing (3ct pack) FDA UDI
- Model / Reference
- 74983 FDA UDI
- Description
- Disposable heat pad for pain relief, non-medicated, apply over-clothing (3ct pack) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00028373749838 FDA UDI
- FDA Product Code
- IMD FDA UDI
- GMDN Term
- Hot/cold therapy pack, single-use 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
No
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: Hot/cold therapy pack, single-use
Beyond BodiHeat® by Okamoto Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Okamoto Usa, Inc.
Sources (1)
- FDA UDI 0372d08d-d479-4dbe-b2c4-d4380109ab87 33 fields · synced May 30, 2026