Primary Device ID | 03760225717936 |
NIH Device Record Key | 75268d17-390a-4bac-9eb7-2a02e3f9db88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TRIWAY |
Version Model Number | N02 00009 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760225717936 [Primary] |
FZX | Guide, Surgical, Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03760225717936]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-01-31 |
Device Publish Date | 2019-03-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TRIWAY 79154341 4702022 Live/Registered |
In2Bones 2014-06-04 |