UDI device identifier
ION AO Coupling Cannulated Handle SR12-5006
UDI device identifier 00081013188039 · Surgentec, LLC
Key facts
| Primary DI | 00081013188039 |
|---|---|
| Brand name | ION AO Coupling Cannulated Handle |
| Version or model | SR12-5006 |
| Company | Surgentec, LLC |
| DUNS number | 004095409 |
| Product code | MRW |
| GMDN term | Facet joint prosthesis |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Mar 9, 2026 |
| Version date | May 5, 2026 |
| Description | SR12- ION Facet Screw System |
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: