UDI device identifier
Verdant GL-CR106GFX
UDI device identifier 00075289232282 · TRANZONIC ACQUISITION CORP.
Key facts
| Primary DI | 00075289232282 |
|---|---|
| Brand name | Verdant |
| Version or model | GL-CR106GFX |
| Catalog number | GL-CR106GFX |
| Company | TRANZONIC ACQUISITION CORP. |
| DUNS number | 090125555 |
| Product code | LZA |
| GMDN term | Polychloroprene examination/treatment glove, non-powdered |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 14, 2022 |
| Version date | Jun 14, 2023 |
| Description | Verdant Disposable Chloroprene Examination Grade Gloves, Powder Free, Green, XLarge, 100/bx, 10bx/cs |
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: