UDI device identifier
Dr. Scholl's 1612171
UDI device identifier 00011017576983 · BAYER HEALTHCARE LLC
Key facts
| Primary DI | 00011017576983 |
|---|---|
| Brand name | Dr. Scholl's |
| Version or model | 1612171 |
| Company | BAYER HEALTHCARE LLC |
| DUNS number | 112117283 |
| Product code | GEH |
| GMDN term | Wart-removal cryogenic kit |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 12, 2018 |
| Version date | Oct 1, 2020 |
| Description | Dr. Scholl's Freeze Away Wart Remover ( blue Box) is a cryosurgical system for the removal of common and plantar warts. The device consists of the following: pressurized canister filled with liquid mixture of dimethyl ether and propane, reusable activator that releases the cryogen into the… |
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: