UDI device identifier
Aspida 51924
UDI device identifier 00190376159645 · ALPHATEC SPINE, INC.
Key facts
| Primary DI | 00190376159645 |
|---|---|
| Brand name | Aspida |
| Version or model | 51924 |
| Company | ALPHATEC SPINE, INC. |
| DUNS number | 602465783 |
| Product code | LXH |
| GMDN term | Orthopaedic bone pin, non-bioabsorbable |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | Yes |
| Publish date | Nov 6, 2019 |
| Version date | Jul 14, 2025 |
| Description | Medial Temporary Fixation Pin |
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: