UDI device identifier
PHARMA-GLOVE-LTC PGNS12-LTC-M
UDI device identifier 00075289715334 · McGowan Enterprises, Inc.
Key facts
| Primary DI | 00075289715334 |
|---|---|
| Brand name | PHARMA-GLOVE-LTC |
| Version or model | PGNS12-LTC-M |
| Catalog number | PGNS12-LTC-M |
| Company | McGowan Enterprises, Inc. |
| DUNS number | 029901019 |
| Product code | KGO |
| GMDN term | Nitrile surgical glove, non-powdered |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Nov 15, 2022 |
| Version date | Feb 12, 2024 |
| Description | SURGICAL EXAM GLOVE, STERILE, NITRILE, 12" LENGTH, CHEMO APPROVED, POWDER FREE, WHITE, MEDIUM |
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: