Primary Device ID | 10841307131342 |
NIH Device Record Key | 78748e85-c3ff-44b0-b196-2636f02c2be6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIRECTguide™ Guided Start Drill |
Version Model Number | GD2.0-6 |
Catalog Number | GD2.0-6 |
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 | 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 |
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 | 10841307131342 [Primary] |
DZI | Drill, Bone, Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
[10841307131342]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-28 |
Device Publish Date | 2024-05-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DIRECTGUIDE 97918054 not registered Live/Pending |
Implant Direct Sybron International LLC 2023-05-03 |
![]() DIRECTGUIDE 74699809 2095674 Dead/Cancelled |
VOGEL SATELLITE TV PUBLISHING INC. 1995-07-11 |