UDI device identifier
CareOne 041520125019
UDI device identifier 00041520125019 · Ahold U.S.A., Inc.
Key facts
| Primary DI | 00041520125019 |
|---|---|
| Brand name | CareOne |
| Version or model | 041520125019 |
| Company | Ahold U.S.A., Inc. |
| DUNS number | 170199058 |
| Product code | LZA |
| GMDN term | Nitrile examination/treatment glove, non-powdered, non-antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 29, 2019 |
| Version date | Aug 19, 2021 |
| Description | Powder Free Nitrile Gloves, 50 single use only gloves (by weight), one size |
At a glance
- None MAUDE reports citing this UDI
- No 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: