Primary Device ID | 03760225716786 |
NIH Device Record Key | 9774cc7e-add0-485d-ad15-fc17d9729335 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEOFUSE |
Version Model Number | V45 ST542 |
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 |
Phone | +33472292626 |
contact@in2bones.com |
Length | 42 Millimeter |
Outer Diameter | 4.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760225716786 [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 | 2019-07-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NEOFUSE 90059115 not registered Live/Pending |
HT Medical, LLC 2020-07-17 |
![]() NEOFUSE 88658051 not registered Live/Pending |
School Specialty, Inc. 2019-10-17 |
![]() NEOFUSE 85620279 4359123 Live/Registered |
EMEMORY TECHNOLOGY INC. 2012-05-09 |
![]() NEOFUSE 85555061 4846300 Live/Registered |
Kennard, Clay 2012-02-28 |
![]() NEOFUSE 79258343 5899860 Live/Registered |
In2Bones 2019-03-12 |
![]() NEOFUSE 77377683 3585548 Dead/Cancelled |
Mesoblast Limited 2008-01-22 |