Primary Device ID | 03701337615642 |
NIH Device Record Key | cf505d6f-47b9-4af9-bca9-c19f05402abb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Triway |
Version Model Number | N20 ST735 |
Catalog Number | N20 ST735 |
Company DUNS | 263616749 |
Company Name | IN2BONES |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03701337615642 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRIWAY 79154341 4702022 Live/Registered |
In2Bones 2014-06-04 |