UDI device identifier
Trestle Luxe 713-1008
UDI device identifier 00190376214894 · ALPHATEC SPINE, INC.
Key facts
| Primary DI | 00190376214894 |
|---|---|
| Brand name | Trestle Luxe |
| Version or model | 713-1008 |
| Company | ALPHATEC SPINE, INC. |
| DUNS number | 602465783 |
| Product code | FZX |
| GMDN term | Surgical drill guide, reusable |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 5, 2020 |
| Version date | Apr 6, 2020 |
| Description | INTRADISCAL DRILL GUIDE, 08MM |
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: