Primary Device ID | 03700780613427 |
NIH Device Record Key | 6e59fbdd-71b8-47cb-9095-f5bbd494f298 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Idys® TLIF |
Version Model Number | 06533307 |
Catalog Number | 06533307 |
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 | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us | |
Phone | +1 773 868 7041 |
s.chambat@clariance-spine.us |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Height | 8 Millimeter |
Depth | 28 Millimeter |
Width | 11 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700780613427 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, 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 | 2025-02-03 |
Device Publish Date | 2025-01-24 |
03700780613519 | TLIF CAGE |
03700780613502 | TLIF CAGE |
03700780613496 | TLIF CAGE |
03700780613489 | TLIF CAGE |
03700780613472 | TLIF CAGE |
03700780613465 | TLIF CAGE |
03700780613458 | TLIF CAGE |
03700780613441 | TLIF CAGE |
03700780613434 | TLIF CAGE |
03700780613427 | TLIF CAGE |
03700780602803 | TLIF CAGE |
03700780602797 | TLIF CAGE |
03700780602780 | TLIF CAGE |
03700780602773 | TLIF CAGE |
03700780602766 | TLIF CAGE |
03700780602759 | TLIF CAGE |
03700780602742 | TLIF CAGE |
03700780602735 | TLIF CAGE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IDYS 79237665 5682795 Live/Registered |
CLARIANCE 2018-04-11 |