DIRECTguide™ Guided Step Drill GSD3.4-16

GUDID 10841307131182

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Fluted surgical drill bit, reusable
Primary Device ID10841307131182
NIH Device Record Key8222a820-58d8-42d7-85e8-ed1208b46877
Commercial Distribution StatusIn Commercial Distribution
Brand NameDIRECTguide™ Guided Step Drill
Version Model NumberGSD3.4-16
Catalog NumberGSD3.4-16
Company DUNS868856969
Company NameIMPLANT DIRECT SYBRON MANUFACTURING LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com
Phone1-888-649-6425
Emailcustomerservice@implantdirect.com

Device Dimensions

Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
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Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110841307131182 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZIDrill, Bone, Powered

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


[10841307131182]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-28
Device Publish Date2024-05-20

On-Brand Devices [DIRECTguide™ Guided Step Drill ]

10841307131182GSD3.4-16
10841307131090GSD2.8-8
10841307131083GSD2.3-16
10841307131052GSD2.3-10

Trademark Results [DIRECTguide]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DIRECTGUIDE
DIRECTGUIDE
97918054 not registered Live/Pending
Implant Direct Sybron International LLC
2023-05-03
DIRECTGUIDE
DIRECTGUIDE
74699809 2095674 Dead/Cancelled
VOGEL SATELLITE TV PUBLISHING INC.
1995-07-11

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