UDI device identifier
Regenacyn Plus Scar Management Hydrogel 84875
UDI device identifier 00189116000071 · Sonoma Pharmaceuticals, Inc.
Key facts
| Primary DI | 00189116000071 |
|---|---|
| Brand name | Regenacyn Plus Scar Management Hydrogel |
| Version or model | 84875 |
| Catalog number | 84875 |
| Company | Sonoma Pharmaceuticals, Inc. |
| DUNS number | 081642964 |
| Product code | PFP |
| GMDN term | Wound hydrogel dressing, non-antimicrobial |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 2, 2022 |
| Version date | Dec 12, 2022 |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: