UDI device identifier
Accu-Chek Safe-T-Pro 03740838001
UDI device identifier 00064562213261 · Roche Diabetes Care GmbH
Key facts
| Primary DI | 00064562213261 |
|---|---|
| Brand name | Accu-Chek Safe-T-Pro |
| Version or model | 03740838001 |
| Catalog number | 03740838001 |
| Company | Roche Diabetes Care GmbH |
| DUNS number | 313212471 |
| Product code | FMK |
| GMDN term | Manual blood lancing device, reusable |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Feb 3, 2023 |
| Version date | Feb 13, 2023 |
| Description | Accu-Chek Safe-T-Pro Plus (CDN, US) |
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: