UDI device identifier
Flex Plus ProM-022
UDI device identifier 00185098000108 · PRO MEDICAL SUPPLIES, INC.
Key facts
| Primary DI | 00185098000108 |
|---|---|
| Brand name | Flex Plus |
| Version or model | ProM-022 |
| Catalog number | ProM-022 |
| Company | PRO MEDICAL SUPPLIES, INC. |
| DUNS number | 135741127 |
| Product code | GXY |
| GMDN term | Transcutaneous electrical stimulation electrode, single-use |
| Premarket submission | K132998 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 26, 2016 |
| Version date | Feb 19, 2021 |
| Description | Electrodes - Flex Plus -2.0" x 2.0" (1 pack = 4 electrodes per pack) |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: