Primary Device ID | 03760225717684 |
NIH Device Record Key | 6ebd5171-cb4f-4efa-b31c-0b0dfe1bb379 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRIWAY |
Version Model Number | N20 ST530 |
Company DUNS | 263616749 |
Company Name | IN2BONES |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 25 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760225717684 [Primary] |
HWC | Screw, Fixation, Bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2019-03-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TRIWAY 79154341 4702022 Live/Registered |
In2Bones 2014-06-04 |