UDI device identifier
Care One 52
UDI device identifier 00041520870902 · Ahold U.S.A., Inc.
Key facts
| Primary DI | 00041520870902 |
|---|---|
| Brand name | Care One |
| Version or model | 52 |
| Company | Ahold U.S.A., Inc. |
| DUNS number | 170199058 |
| Product code | LPN |
| GMDN term | Multi-purpose soft/rigid contact lens solution |
| Device class | Class II |
| Single use | No |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jan 29, 2021 |
| Version date | Feb 8, 2021 |
| Description | Sterile 3% Hydrogen Peroxide (Lens Care System) |
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: