Primary Device ID | 03700780644193 |
NIH Device Record Key | 940b4186-4b71-4992-97cb-50d7a5e2b28d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Idys®- C ZP 3DTi |
Version Model Number | 44063516-S |
Catalog Number | 44063516-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 | 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 | +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 |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Length | 16 Millimeter |
Outer Diameter | 3.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03700780644193 [Primary] |
OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-04 |
Device Publish Date | 2024-03-27 |
03700780644001 | GIMBAL |
03700780643837 | ANGULATED PUNCH RETRACTABLE |
03700780643820 | RETRACTABLE PUNCH |
03700780644216 | SCREW |
03700780644209 | SCREW |
03700780644193 | SCREW |
03700780644186 | SCREW |
03700780644049 | SCREW |
03700780644032 | SCREW |
03700780644025 | SCREW |
03700780644018 | SCREW |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() IDYS 79237665 5682795 Live/Registered |
CLARIANCE 2018-04-11 |