UDI device identifier
DermaThin XXL
UDI device identifier 00038054654313 · SHOWA BEST GLOVE, INC.
Key facts
| Primary DI | 00038054654313 |
|---|---|
| Brand name | DermaThin |
| Version or model | XXL |
| Catalog number | M7002PFXXL |
| Company | SHOWA BEST GLOVE, INC. |
| DUNS number | 807930412 |
| Product code | LZA |
| GMDN term | Nitrile examination/treatment glove, non-powdered, non-antimicrobial |
| Premarket submission | K211003 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 31, 2023 |
| Version date | Apr 10, 2023 |
| Description | SHOWA, DermaThin® Nitrile PF Exam Biodegradable with Eco Best Technology® (EBT), Chemo claim, fingertip textured, Blue, XXL |
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: