Primary Device ID | 10841307100041 |
NIH Device Record Key | 1df446eb-a7cf-40b4-a821-5490a9ec5741 |
Commercial Distribution Discontinuation | 2021-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GoDirect® Implant |
Version Model Number | 423013 |
Catalog Number | 423013 |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
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 | true |
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 | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com | |
Phone | 1-888-649-6425 |
customerservice@implantdirect.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841307100041 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-02-18 |
Device Publish Date | 2015-09-14 |
10841307121978 | 3.0mmD x 8mmL, 1.5mm Height |
10841307122241 | 3.7mmD x 8mmL, 3.0mm Height |
10841307122067 | 3.7mmD x 8mmL, 1.5mm Height |
10841307100041 | 3.0mmD x 13mmL, 1.5mm Height |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() GODIRECT 88213357 5793539 Live/Registered |
Associates for the Advancement of Musculoskeletal Innovation, Inc. 2018-12-01 |
![]() GODIRECT 87326482 5295254 Live/Registered |
Honeywell International Inc. 2017-02-07 |
![]() GODIRECT 86825571 5247109 Live/Registered |
Honeywell International Inc. 2015-11-19 |
![]() GODIRECT 86664931 4931272 Live/Registered |
Plavan Commercial Fueling, Inc. 2015-06-17 |
![]() GODIRECT 86014421 not registered Dead/Abandoned |
CORE ORTHOPAEDICS, INC. 2013-07-18 |
![]() GODIRECT 85395850 4141754 Live/Registered |
Implant Direct Sybron International LLC 2011-08-11 |
![]() GODIRECT 77961974 3972491 Dead/Cancelled |
eWinWin, Inc. 2010-03-18 |