UDI device identifier
Vermed SHRP18 GAL PHARMA W/PORT/DUO LID
UDI device identifier 00009336006533 · GRAPHIC CONTROLS ACQUISITION CORP
Key facts
| Primary DI | 00009336006533 |
|---|---|
| Brand name | Vermed |
| Version or model | SHRP18 GAL PHARMA W/PORT/DUO LID |
| Catalog number | 32028116 |
| 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 | Jan 24, 2017 |
| Version date | Aug 18, 2023 |
| Description | SHRP18 GAL PHARMA W/PORT/DUO LID |
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: