SCLERAL FIXATION TWIST HOOK 1643928

GUDID 00192896072893

SCLERAL FIXATION TWIST HOOK RIGHT HANDLED CROSSED TIPS

SONTEC INSTRUMENTS, INC.

Ocular hook/spatula/manipulator, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable Eye muscle hook, reusable
Primary Device ID00192896072893
NIH Device Record Key77d394b7-bef0-4714-b275-01b2d4391c22
Commercial Distribution StatusIn Commercial Distribution
Brand NameSCLERAL FIXATION TWIST HOOK
Version Model Number1643928
Catalog Number1643928
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

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896072893 [Primary]

FDA Product Code

HNQHook, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896072893]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-24
Device Publish Date2018-10-08

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