UDI device identifier
Care One 67-50K
UDI device identifier 00041520105134 · Ahold U.S.A., Inc.
Key facts
| Primary DI | 00041520105134 |
|---|---|
| Brand name | Care One |
| Version or model | 67-50K |
| Company | Ahold U.S.A., Inc. |
| DUNS number | 170199058 |
| Product code | DQA |
| GMDN term | Pulse oximeter probe, reusable |
| Premarket submission | K082641 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 23, 2021 |
| Version date | Oct 7, 2024 |
| Description | Care One Pulse Oximeter |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: