UDI device identifier
3M™ ACE™ Brand 906001
UDI device identifier 00051131192430 · 3M Company
Key facts
| Primary DI | 00051131192430 |
|---|---|
| Brand name | 3M™ ACE™ Brand |
| Version or model | 906001 |
| Catalog number | 906001 |
| Company | 3M Company |
| DUNS number | 178590899 |
| Product code | IMD |
| GMDN term | Musculoskeletal hot/cold therapy pack, reusable |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 25, 2018 |
| Version date | Jan 12, 2026 |
| Description | ACE™ Brand Instant Cold Compress 906001 |
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: