UDI device identifier
Compound W® CWUS004502, CWUS004103, CWUS004602
UDI device identifier 00075137000032 · Medtech Products Inc.
Key facts
| Primary DI | 00075137000032 |
|---|---|
| Brand name | Compound W® |
| Version or model | CWUS004502, CWUS004103, CWUS004602 |
| Company | Medtech Products Inc. |
| DUNS number | 060272465 |
| Product code | GEH |
| GMDN term | Wart-removal cryogenic kit |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 16, 2018 |
| Version date | Jun 26, 2025 |
| Description | Compound W® Nitrofreeze™ Nitrous Oxide Wart Removal System |
At a glance
- None MAUDE reports citing this UDI
- No 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: