GUIDE FIXTURE DRIVER

GUDID 08800020849359

SNUCONE Co.,LTD.

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable
Primary Device ID08800020849359
NIH Device Record Keyd2b7755b-4210-4089-a51c-ab2e7c7a84be
Commercial Distribution StatusIn Commercial Distribution
Brand NameGUIDE FIXTURE DRIVER
Version Model NumberGFGDA
Company DUNS688806132
Company NameSNUCONE Co.,LTD.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com
Phone9999999999
Emailsnucone@naver.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108800020849359 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


[08800020849359]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-01
Device Publish Date2023-02-21

On-Brand Devices [GUIDE FIXTURE DRIVER]

08800020849359GFGDA
08800020849342GFGDAM

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