UDI device identifier
Kelo-cote Advanced Formula Scar Gel Lot Code
UDI device identifier 00070030511746 · Alliance Pharma Inc.
Key facts
| Primary DI | 00070030511746 |
|---|---|
| Brand name | Kelo-cote Advanced Formula Scar Gel |
| Version or model | Lot Code |
| Company | Alliance Pharma Inc. |
| DUNS number | 081138954 |
| Product code | MDA |
| GMDN term | Scar-management dressing, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 10, 2024 |
| Version date | Apr 18, 2024 |
| Description | Kelo-cote Advanced Formula Scar Gel 10g |
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: