UDI device identifier
MEDI 24002017
UDI device identifier 00013964463286 · MEDI MANUFACTURING, INC.
Key facts
| Primary DI | 00013964463286 |
|---|---|
| Brand name | MEDI |
| Version or model | 24002017 |
| Company | MEDI MANUFACTURING, INC. |
| DUNS number | 960754430 |
| Product code | MDR |
| GMDN term | Compression bandaging kit |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 20, 2018 |
| Version date | Jun 10, 2022 |
| Description | ***DISC*CURES - STANDARD |
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: