UDI device identifier
Flents K30
UDI device identifier 00077602000301 · APOTHECARY PRODUCTS, LLC
Key facts
| Primary DI | 00077602000301 |
|---|---|
| Brand name | Flents |
| Version or model | K30 |
| Company | APOTHECARY PRODUCTS, LLC |
| DUNS number | 092312735 |
| Product code | EWD |
| GMDN term | Earplugs, single-use |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 28, 2020 |
| Version date | Jun 10, 2022 |
| Description | FLENTS SOFT FOAM EARPLUG |
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: