UDI device identifier
PM-355 PM-355
UDI device identifier 00185098000290 · PRO MEDICAL SUPPLIES, INC.
Key facts
| Primary DI | 00185098000290 |
|---|---|
| Brand name | PM-355 |
| Version or model | PM-355 |
| Catalog number | PM-355 |
| Company | PRO MEDICAL SUPPLIES, INC. |
| DUNS number | 135741127 |
| Product code | IPF |
| GMDN term | Transcutaneous electrical stimulation electrode, single-use |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 24, 2016 |
| Version date | Feb 19, 2021 |
| Description | (1) -Transcutaneous Nerve Stimulator -Three Mode with Timer Dual Channel 4 Leads - Zipper Case Includes: device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual |
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: