UDI device identifier
Bausch + Lomb 5509
UDI device identifier 00047144055091 · Bausch & Lomb Incorporated
Key facts
| Primary DI | 00047144055091 |
|---|---|
| Brand name | Bausch + Lomb |
| Version or model | 5509 |
| Catalog number | FCP-4123 |
| Company | Bausch & Lomb Incorporated |
| DUNS number | 196603781 |
| Product code | MRC |
| GMDN term | Contact lens wetting solution |
| Device class | Class II |
| Single use | No |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 17, 2018 |
| Version date | May 15, 2024 |
| Description | Rigid Gas Permeable Contact Lens Rewetting Drops. 0.33 FL OZ |
At a glance
- None MAUDE reports citing this UDI
- No 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: