UDI device identifier
Vermed SHRPSHARPS BIO 5Q/5L YELLOW, SQUARE
UDI device identifier 00009336008704 · GRAPHIC CONTROLS ACQUISITION CORP
Key facts
| Primary DI | 00009336008704 |
|---|---|
| Brand name | Vermed |
| Version or model | SHRPSHARPS BIO 5Q/5L YELLOW, SQUARE |
| Catalog number | 32028543 |
| Company | GRAPHIC CONTROLS ACQUISITION CORP |
| DUNS number | 002111896 |
| Product code | MMK |
| GMDN term | Cytotoxic waste container |
| Premarket submission | K071517 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 1, 2017 |
| Version date | Aug 18, 2023 |
| Description | SHRPSHARPS BIO 5Q/5L YELLOW, SQUARE |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: