GANS SEVERIN CYCLED CANNULA 16-6085

GUDID 00192896019249

GANS SEVERIN CYCLED CANNULA LEFT SIDE OPENING

SONTEC INSTRUMENTS, INC.

Ophthalmic working-channel cannula, reusable
Primary Device ID00192896019249
NIH Device Record Key67f1b063-be50-41e1-8dfb-f91a095568e9
Commercial Distribution StatusIn Commercial Distribution
Brand NameGANS SEVERIN CYCLED CANNULA
Version Model Number16-6085
Catalog Number16-6085
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896019249 [Primary]

FDA Product Code

HMXCannula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896019249]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-19
Device Publish Date2018-09-18

On-Brand Devices [GANS SEVERIN CYCLED CANNULA]

00192896075054GANS SEVERIN CYCLED CANNULA RIGHT SIDE OPENING
00192896019249GANS SEVERIN CYCLED CANNULA LEFT SIDE OPENING

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