Primary Device ID | 10841307131373 |
NIH Device Record Key | 2f8f4a8a-5fbe-4c02-9394-a0654db77df9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DIRECTguide™ 3.5 Platform Hex Driver |
Version Model Number | 3.5HPD |
Catalog Number | 3.5HPD |
Company DUNS | 868856969 |
Company Name | IMPLANT DIRECT SYBRON MANUFACTURING LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10841307131373 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
Moist Heat or Steam Sterilization
[10841307131373]
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 |