UDI device identifier
Flents 65200
UDI device identifier 00025715652009 · APOTHECARY PRODUCTS, LLC
Key facts
| Primary DI | 00025715652009 |
|---|---|
| Brand name | Flents |
| Version or model | 65200 |
| Company | APOTHECARY PRODUCTS, LLC |
| DUNS number | 092312735 |
| Product code | HED |
| GMDN term | Vaginal douche, reusable |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 16, 2020 |
| Version date | Nov 24, 2020 |
| Description | FLENTS DOUCHE KIT |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: