UDI device identifier
DUREX® Air Regular Fit; DUREX® Air 00067981087970
UDI device identifier 00067981087970 · RECKITT BENCKISER LLC
Key facts
| Primary DI | 00067981087970 |
|---|---|
| Brand name | DUREX® Air Regular Fit; DUREX® Air |
| Version or model | 00067981087970 |
| Company | RECKITT BENCKISER LLC |
| DUNS number | 094405024 |
| Product code | HIS |
| GMDN term | Basic male condom, Hevea-latex |
| Premarket submission | K222068 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 13, 2025 |
| Version date | Jun 15, 2026 |
| Description | Durex Air Regular Fit Condom 3ct. Durex Air Condom 3ct. |
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: