UDI device identifier
Mepitel® Film 296288
UDI device identifier 00050428594353 · Mölnlycke Health Care AB
Key facts
| Primary DI | 00050428594353 |
|---|---|
| Brand name | Mepitel® Film |
| Version or model | 296288 |
| Company | Mölnlycke Health Care AB |
| DUNS number | 631770658 |
| Product code | NAD |
| GMDN term | Synthetic polymer semi-permeable film dressing, wound-nonadherent |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 18, 2020 |
| Version date | Jan 13, 2025 |
| Description | Mepitel Film 4x4,8in/10x12cm, CVS |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: