Primary Device ID | 05055343834596 |
NIH Device Record Key | dba309a0-1ac4-439e-b3ba-1c365079821c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Corifix Ligament Anchor Soft Screw |
Version Model Number | 408.135 |
Catalog Number | 408.135 |
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 |
lucinda.gerber@coringroup.com | |
Phone | +441285659866 |
lucinda.gerber@coringroup.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055343834596 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | true |
[05055343834596]
Radiation Sterilization
[05055343834596]
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 |