UDI device identifier
Action® Head Pad
UDI device identifier 00089904000804 · ACTION PRODUCTS, INC.
Key facts
| Primary DI | 00089904000804 |
|---|---|
| Brand name | Action® |
| Version or model | Head Pad |
| Catalog number | 40217-P |
| Company | ACTION PRODUCTS, INC. |
| DUNS number | 067543058 |
| Product code | FMP |
| GMDN term | Freestanding headrest, reusable |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 14, 2021 |
| Version date | Jan 22, 2021 |
| Description | Pediatric Ophthalmic Cradle Headrest |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: