UDI device identifier
DMV Vented Scleral Cup 110
UDI device identifier 00080875971100 · DMV CORPORATION
Key facts
| Primary DI | 00080875971100 |
|---|---|
| Brand name | DMV Vented Scleral Cup |
| Version or model | 110 |
| Catalog number | 110 |
| Company | DMV CORPORATION |
| DUNS number | 084436906 |
| Product code | KYE |
| GMDN term | Rigid contact lens inserter/remover |
| Premarket submission | K830496 |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 6, 2020 |
| Version date | May 12, 2020 |
| Description | Contact lens Inserter with air channel for inserting hybrid, large soft and gp contact lenses. No suction |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: