GANS SEVERIN CYCLED CANNULA 16-6086

GUDID 00192896075054

GANS SEVERIN CYCLED CANNULA RIGHT SIDE OPENING

SONTEC INSTRUMENTS, INC.

Ophthalmic working-channel cannula, reusable
Primary Device ID00192896075054
NIH Device Record Key3a7a1c7c-c5d3-4b00-bba9-8d1121922209
Commercial Distribution StatusIn Commercial Distribution
Brand NameGANS SEVERIN CYCLED CANNULA
Version Model Number16-6086
Catalog Number16-6086
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

Needle Gauge19 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896075054 [Primary]

FDA Product Code

HMXCannula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896075054]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-20

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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