| Primary Device ID | 05055343834602 |
| NIH Device Record Key | 19f69794-d5ca-4591-8813-43970655610d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Corifix Ligament Anchor Soft Screw |
| Version Model Number | 408.720 |
| Catalog Number | 408.720 |
| Company DUNS | 295437313 |
| Company Name | CORIN LTD |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Phone | +441285659866 |
| rachel.king@coringroup.com | |
| Phone | +441285659866 |
| rachel.king@coringroup.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05055343834602 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[05055343834602]
Radiation Sterilization
[05055343834602]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-17 |
| 05055343834718 | SOFT SCREW |
| 05055343834701 | SOFT SCREW |
| 05055343834695 | SOFT SCREW |
| 05055343834688 | SOFT SCREW |
| 05055343834671 | SOFT SCREW |
| 05055343834664 | SOFT SCREW |
| 05055343834657 | SOFT SCREW |
| 05055343834640 | SOFT SCREW |
| 05055343834633 | SOFT SCREW |
| 05055343834626 | SOFT SCREW |
| 05055343834619 | SOFT SCREW |
| 05055343834602 | SOFT SCREW |
| 05055343834596 | SOFT SCREW |
| 05055343834589 | SOFT SCREW |
| 05055343834572 | SOFT SCREW |
| 05055343834565 | SOFT SCREW |