BODIAN LACRIMAL PROBE SET 16-2596

GUDID 00192896018693

BODIAN LACRIMAL PROBE SET CURVED BLUNT PROBE SILICONE TUBE

SONTEC INSTRUMENTS, INC.

Lacrimal probe, reusable
Primary Device ID00192896018693
NIH Device Record Keycc4318ce-59d2-412e-b846-547049d26e6b
Commercial Distribution StatusIn Commercial Distribution
Brand NameBODIAN LACRIMAL PROBE SET
Version Model Number16-2596
Catalog Number16-2596
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 Identifiers

Device Issuing AgencyDevice ID
GS100192896018693 [Primary]

FDA Product Code

HNLProbe, lachrymal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896018693]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-10-28
Device Publish Date2018-09-17

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