Primary Device ID | 03700780629091 |
NIH Device Record Key | ef752289-35ca-47e1-b325-3ac9501a700c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Idys®-ALIF TiVac |
Version Model Number | 42521206-S |
Catalog Number | 42521206-S |
Company DUNS | 296568400 |
Company Name | CLARIANCE |
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 | true |
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 | +1 773 868 7041 |
s.chambat@clariance-spine.us |
Width | 35 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700780629091 [Primary] |
OVD | Intervertebral fusion device with integrated fixation, lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-23 |
Device Publish Date | 2019-12-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IDYS 79237665 5682795 Live/Registered |
CLARIANCE 2018-04-11 |