KUGLEN IRIS/LENS MANIPULATING HOOK 1424782

GUDID 00192896072855

KUGLEN IRIS/LENS MANIPULATING HOOK PUSH-PULL MODEL STRAIGHT TIP STAINLESS STEEL

SONTEC INSTRUMENTS, INC.

Ocular hook/spatula/manipulator, reusable
Primary Device ID00192896072855
NIH Device Record Key1d7fc4da-6d71-4946-90c3-da26c0a18a27
Commercial Distribution StatusIn Commercial Distribution
Brand NameKUGLEN IRIS/LENS MANIPULATING HOOK
Version Model Number1424782
Catalog Number1424782
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
GS100192896072855 [Primary]

FDA Product Code

HNQHook, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896072855]

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 Date2018-10-08

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