UDI device identifier
Precision Xceed Pro 70935
UDI device identifier 00093815709350 · ABBOTT DIABETES CARE INC
Key facts
| Primary DI | 00093815709350 |
|---|---|
| Brand name | Precision Xceed Pro |
| Version or model | 70935 |
| Catalog number | 70935 |
| Company | ABBOTT DIABETES CARE INC |
| DUNS number | 966390890 |
| Product code | NBW |
| GMDN term | Multiple clinical chemistry analyte monitoring system IVD, point-of-care |
| Premarket submission | K080960 |
| Device class | 1 | 2 |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 22, 2016 |
| Version date | Dec 11, 2019 |
| Description | Precision Xceed Pro Blood ß-Ketone Test Strips |
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: