UDI device identifier
Beyond BodiHeat® 74982
UDI device identifier 00028373749821 · OKAMOTO USA, INC.
Key facts
| Primary DI | 00028373749821 |
|---|---|
| Brand name | Beyond BodiHeat® |
| Version or model | 74982 |
| Company | OKAMOTO USA, INC. |
| DUNS number | 175752724 |
| Product code | IMD |
| GMDN term | Musculoskeletal hot/cold therapy pack, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 26, 2020 |
| Version date | Jan 12, 2026 |
| Description | Disposable heat pad for pain relief, non-medicated, apply over-clothing (1ct packed in 24ct display box) |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: