Primary Device ID | 10841307108719 |
NIH Device Record Key | 552dca5b-2a63-4775-9d0f-3566f6a1ffb4 |
Commercial Distribution Discontinuation | 2019-05-22 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Dual-Grip™ Extra Long Fixation Screw (2 pieces) |
Version Model Number | 1000-12XL |
Catalog Number | 1000-12XL |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
Device Count | 2 |
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 | false |
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 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841307108712 [Unit of Use] |
GS1 | 10841307108719 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307108719]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-09-14 |
10841307108719 | 1000-12XL |
10841307108696 | 1000-11XL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DUAL-GRIP 90241709 not registered Live/Pending |
Power Stop LLC 2020-10-08 |
![]() DUAL-GRIP 85117881 3954407 Live/Registered |
Sofa Mart, LLC 2010-08-27 |
![]() DUAL-GRIP 78522795 3252310 Live/Registered |
CONTITECH USA, INC. 2004-11-24 |