UDI device identifier
DUREX Extra Sensitive Stimulating Condom Condom
UDI device identifier 00067981160475 · RB Health (us) LLC
Key facts
| Primary DI | 00067981160475 |
|---|---|
| Brand name | DUREX Extra Sensitive Stimulating Condom |
| Version or model | Condom |
| Company | RB Health (us) LLC |
| DUNS number | 081049410 |
| Product code | HIS |
| GMDN term | Basic male condom, Hevea-latex |
| Premarket submission | K040185 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 9, 2020 |
| Version date | Apr 17, 2020 |
| Description | Condom |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: