Primary Device ID | 05055196994539 |
NIH Device Record Key | 5ff15648-e183-4ac3-b37a-4609c7fe5097 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Corifix Ligament Anchor Screw |
Version Model Number | 165.300 |
Catalog Number | 165.300 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055196994539 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | true |
[05055196994539]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-01-08 |
Device Publish Date | 2016-08-17 |
05055343880203 | LIGAMENT ANCHOR |
05055196994546 | LIGAMENT CLAW |
05055196994539 | LIGAMENT CLAW |
05055196994515 | LIGAMENT ANCHOR |
05055196994508 | LIGAMENT ANCHOR |
05055196994492 | LIGAMENT ANCHOR |
05055196994485 | LIGAMENT ANCHOR |
05055196986831 | BONE SCREW |
05055196986824 | BONE SCREW |
05055196986817 | BONE SCREW |
05055196986800 | BONE SCREW |
05055196986794 | BONE SCREW |
05055196986787 | BONE SCREW |
05055196986770 | BONE SCREW |
05055196986763 | BONE SCREW |
05055196986756 | BONE SCREW |
05055196986749 | BONE SCREW |