| Primary Device ID | 06009544009320 |
| NIH Device Record Key | f3e916e5-d85b-401a-b15b-e89627d98d13 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tri-Nex Co-Axis™ |
| Version Model Number | IA50-12D-11.5 |
| Company DUNS | 636239584 |
| Company Name | SOUTHERN IMPLANTS (PTY) LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06009544009320 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-08 |
| Device Publish Date | 2019-01-08 |
| 06009544009344 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø5.0 x 16.5mm |
| 06009544009337 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø5.0 x 13.5mm |
| 06009544009320 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø5.0 x 12mm |
| 06009544009313 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø5.0 x 10.5mm |
| 06009544009306 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø4.3 x 16.5mm |
| 06009544009290 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø4.3 x 13.5mm |
| 06009544009283 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø4.3 x 12mm |
| 06009544009276 | Tri-Nex Tapered Implant, 12° Co-Axis™, Ø4.3 x 10.5mm |