DIRECTguide™ Sleeve Regular GSR

GUDID 10841307132141

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Instrument tray, reusable
Primary Device ID10841307132141
NIH Device Record Key26689e0f-42a2-4739-85ae-aa6869e12021
Commercial Distribution StatusIn Commercial Distribution
Brand NameDIRECTguide™ Sleeve Regular
Version Model NumberGSR
Catalog NumberGSR
Company DUNS868856969
Company NameIMPLANT DIRECT SYBRON MANUFACTURING LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
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 Identifiers

Device Issuing AgencyDevice ID
GS110841307132141 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


[10841307132141]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-10
Device Publish Date2025-01-31

On-Brand Devices [DIRECTguide™ Sleeve Regular]

10841307128601GSR
10841307132141GSR

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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