UDI device identifier
ProWorks GL-V104FM
UDI device identifier 00075289132131 · TRANZONIC COMPANIES, THE
Key facts
| Primary DI | 00075289132131 |
|---|---|
| Brand name | ProWorks |
| Version or model | GL-V104FM |
| Catalog number | GL-V104FM |
| Company | TRANZONIC COMPANIES, THE |
| DUNS number | 007900020 |
| Product code | LYZ |
| GMDN term | Vinyl examination/treatment glove, non-powdered |
| Premarket submission | K072227 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 2, 2020 |
| Version date | Jun 15, 2023 |
| Description | ProWorks® Disposable Vinyl Exam Grade Gloves, Powder Free, Clear, 4 mil, Medium, 100/bx, 10 bxs/cs |
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: