UDI device identifier
PROTECT 800 PROSNCG-XL
UDI device identifier 00075289715235 · McGowan Enterprises, Inc.
Key facts
| Primary DI | 00075289715235 |
|---|---|
| Brand name | PROTECT 800 |
| Version or model | PROSNCG-XL |
| Catalog number | PROSNCG-XL |
| Company | McGowan Enterprises, Inc. |
| DUNS number | 029901019 |
| Product code | OPJ |
| GMDN term | Nitrile surgical glove, non-powdered |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 21, 2022 |
| Version date | Dec 29, 2022 |
| Description | SURGICAL GLOVE, STERILE, NITRILE, 12" LENGTH, CHEMO TESTED, POWDER FREE, WHITE, X-LARGE |
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: