UDI device identifier
MUELLER PRO STRIPS PRE-CUT/ELBOW 410954
UDI device identifier 00074676419541 · Mueller Sports Medicine, Inc.
Key facts
| Primary DI | 00074676419541 |
|---|---|
| Brand name | MUELLER PRO STRIPS PRE-CUT/ELBOW |
| Version or model | 410954 |
| Catalog number | 410954 |
| Company | Mueller Sports Medicine, Inc. |
| DUNS number | 006426316 |
| Product code | FQM |
| GMDN term | Skin-cover adhesive strip, non-antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 15, 2022 |
| Version date | Oct 24, 2022 |
| Description | PRO STRIPS PRE-CUT/ELBOW, S/C 12 EA |
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: