UDI device identifier
DeScribe Transparent PFD Patch 5035837
UDI device identifier 00186295000359 · MERZ NORTH AMERICA, INC.
Key facts
| Primary DI | 00186295000359 |
|---|---|
| Brand name | DeScribe Transparent PFD Patch |
| Version or model | 5035837 |
| Company | MERZ NORTH AMERICA, INC. |
| DUNS number | 028147846 |
| Product code | PKO |
| GMDN term | Synthetic polymer semi-permeable film dressing, adhesive, non-sterile |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 6, 2017 |
| Version date | Mar 29, 2018 |
| Description | Individually packaged DeScribe PFD Patch (each) |
At a glance
- 1–9 MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: