UDI device identifier
Indus® 01-71006-63
UDI device identifier 00190361001348 · SPINEFRONTIER, INC.
Key facts
| Primary DI | 00190361001348 |
|---|---|
| Brand name | Indus® |
| Version or model | 01-71006-63 |
| Company | SPINEFRONTIER, INC. |
| DUNS number | 002003243 |
| Product code | KWQ |
| GMDN term | Spinal fixation plate, non-bioabsorbable |
| Premarket submission | K121060 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | Yes |
| Publish date | Apr 15, 2016 |
| Version date | Nov 20, 2025 |
| Description | Invue Max, Three Level ACP, 63mm |
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: