UDI device identifier
HOMEDICS SR-CMXC10HJ
UDI device identifier 00031262110541 · FKA DISTRIBUTING CO., LLC
Key facts
| Primary DI | 00031262110541 |
|---|---|
| Brand name | HOMEDICS |
| Version or model | SR-CMXC10HJ |
| Company | FKA DISTRIBUTING CO., LLC |
| DUNS number | 183280973 |
| Product code | IRP |
| GMDN term | Pneumatic massager |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 10, 2023 |
| Version date | Aug 18, 2023 |
| Description | Battery + Calf Wrap "Combo" |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: