UDI device identifier
HALYARD SGL85055B
UDI device identifier 00076490718282 · Ansell
Key facts
| Primary DI | 00076490718282 |
|---|---|
| Brand name | HALYARD |
| Version or model | SGL85055B |
| Catalog number | SGL85055B |
| Company | Ansell |
| DUNS number | 120522524 |
| Product code | KGO |
| GMDN term | Polychloroprene surgical glove, non-powdered |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jul 19, 2024 |
| Version date | Jul 29, 2024 |
| Description | HALYARD SGL85055B Neoprene Micro Bulk Size (5.5), Powder-Free Neoprene Surgical Glove |
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: