UDI device identifier
Rapid Relief Cold 31259
UDI device identifier 00064317312591 · Rapid Aid Corp
Key facts
| Primary DI | 00064317312591 |
|---|---|
| Brand name | Rapid Relief Cold |
| Version or model | 31259 |
| Company | Rapid Aid Corp |
| DUNS number | 241235050 |
| 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 | Feb 8, 2021 |
| Version date | Jan 12, 2026 |
| Description | Rapid Relief Instant Cold Pack (single use) |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- Yes 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: