UDI device identifier
Trojan™ Sensitivity Pack 00022600001492
UDI device identifier 00022600001492 · CHURCH & DWIGHT CO., INC.
Key facts
| Primary DI | 00022600001492 |
|---|---|
| Brand name | Trojan™ Sensitivity Pack |
| Version or model | 00022600001492 |
| Company | CHURCH & DWIGHT CO., INC. |
| DUNS number | 001211952 |
| Product code | HIS |
| GMDN term | Basic male condom, Hevea-latex |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 28, 2019 |
| Version date | Oct 3, 2022 |
| Description | Pack includes: Ultra Thin, Her Pleasure Ecstasy, Ultra ENZ and Thintensity. |
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: