| Primary Device ID | 05055343834633 | 
| NIH Device Record Key | 7932005d-84d2-4fc1-9641-d8cbca6fef1c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Corifix Ligament Anchor Soft Screw | 
| Version Model Number | 408.735 | 
| Catalog Number | 408.735 | 
| 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 | 05055343834633 [Primary] | 
| HWC | Screw, fixation, bone | 
| Steralize Prior To Use | true | 
| Device Is Sterile | true | 
[05055343834633]
Radiation Sterilization
[05055343834633]
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 |