LASIK SPATULA T12-1442

GUDID 00192896072589

LASIK SPATULA SINGLE ENDED SEMI-SHARP TIP TITANIUM

SONTEC INSTRUMENTS, INC.

Ocular hook/spatula/manipulator, reusable
Primary Device ID00192896072589
NIH Device Record Key00865d75-6b2c-4a3c-ab16-8fa8165354e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameLASIK SPATULA
Version Model NumberT12-1442
Catalog NumberT12-1442
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 Latexfalse
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
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896072589 [Primary]

FDA Product Code

HNDSpatula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072589]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2018-09-19

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