UDI device identifier
Compound W® CW067601; CW067201; CW067202; CW068101 (First Aid)
UDI device identifier 00075137110854 · Medtech Products Inc.
Key facts
| Primary DI | 00075137110854 |
|---|---|
| Brand name | Compound W® |
| Version or model | CW067601; CW067201; CW067202; CW068101 (First Aid) |
| Company | Medtech Products Inc. |
| DUNS number | 060272465 |
| Product code | GEH |
| GMDN term | Wart-removal cryogenic kit |
| Premarket submission | K161294 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 9, 2017 |
| Version date | Jun 26, 2025 |
| Description | COMPOUND W® DUAL POWER (2-in-1 Treatment Kit for Large Warts) |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: