UDI device identifier
Flents 70129
UDI device identifier 00023185000276 · APOTHECARY PRODUCTS, LLC
Key facts
| Primary DI | 00023185000276 |
|---|---|
| Brand name | Flents |
| Version or model | 70129 |
| Company | APOTHECARY PRODUCTS, LLC |
| DUNS number | 092312735 |
| Product code | LRX |
| GMDN term | Contact lens case |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 8, 2018 |
| Version date | Nov 8, 2018 |
| Description | Soft Grip Contact Lens Cases |
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: