UDI device identifier
Sure-Vue T3018-7533
UDI device identifier 00006136471295 · FISHER SCIENTIFIC COMPANY L.L.C.
Key facts
| Primary DI | 00006136471295 |
|---|---|
| Brand name | Sure-Vue |
| Version or model | T3018-7533 |
| Catalog number | 23046386 |
| Company | FISHER SCIENTIFIC COMPANY L.L.C. |
| DUNS number | 004321519 |
| Product code | DHR |
| GMDN term | Rheumatoid factor IVD, kit, agglutination |
| Premarket submission | K910539 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 27, 2017 |
| Version date | Jul 6, 2018 |
| Description | SURE-VUE RF 500 TESTS |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: