ScrewRedirect® Guide Pin 5037-07

GUDID 10841307119159

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implantation depth/angle gauge, reusable
Primary Device ID10841307119159
NIH Device Record Key05108562-0658-4a8d-a24d-6ef5d6c26add
Commercial Distribution StatusIn Commercial Distribution
Brand NameScrewRedirect® Guide Pin
Version Model Number5037-07
Catalog Number5037-07
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 Kitfalse
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
Email[email protected]

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110841307119159 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10841307119159]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-11-27
Device Publish Date2015-12-29

On-Brand Devices [ScrewRedirect® Guide Pin]

108413071191735057-07
108413071191665047-07
108413071191595037-07

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