UDI device identifier
WINK CLOSER 14998
UDI device identifier 00028373149980 · OKAMOTO USA, INC.
Key facts
| Primary DI | 00028373149980 |
|---|---|
| Brand name | WINK CLOSER |
| Version or model | 14998 |
| Company | OKAMOTO USA, INC. |
| DUNS number | 175752724 |
| Product code | HIS |
| GMDN term | Basic male condom, Hevea-latex |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 6, 2024 |
| Version date | Sep 16, 2024 |
| Description | WINK Closer Condom (1008 pc case) |
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: