Primary Device ID | 03760225717660 |
NIH Device Record Key | 28385110-dbb8-410b-b1f4-8d212c518296 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRIWAY |
Version Model Number | N20 ST223 |
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 | 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 |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Length | 250 Millimeter |
Outer Diameter | 12 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760225717660 [Primary] |
HSB | Rod, Fixation, Intramedullary And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-12-08 |
Device Publish Date | 2019-03-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TRIWAY 79154341 4702022 Live/Registered |
In2Bones 2014-06-04 |