Kirby Expressor

GUDID 00192896109964

Kirby Expressor And Flat Zonule Separator Double-Ended

SONTEC INSTRUMENTS, INC.

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Primary Device ID00192896109964
NIH Device Record Key4da501d3-03ba-41dd-ac42-76a15af08365
Commercial Distribution StatusIn Commercial Distribution
Brand NameKirby Expressor
Version Model Number12-4465
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch
Length5.75 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896109964 [Primary]

FDA Product Code

HNDSpatula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896109964]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-03
Device Publish Date2021-05-26

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