UDI device identifier
AllCare EF601X
UDI device identifier 00182921000397 · ALLCARE, INC
Key facts
| Primary DI | 00182921000397 |
|---|---|
| Brand name | AllCare |
| Version or model | EF601X |
| Catalog number | EF601X |
| Company | ALLCARE, INC |
| DUNS number | 362187580 |
| Product code | KME |
| GMDN term | Basic bed sheet, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 27, 2022 |
| Version date | Dec 5, 2022 |
| Description | FITTED SHEET 32" X 90" LIGHT BLUE, DISPOSABLE |
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: