CRAWFORD LACRIMAL INTUBATION SET 16-2594

GUDID 00192896018686

CRAWFORD LACRIMAL INTUBATION SET OLIVE PROBE SILICONE TUBE

SONTEC INSTRUMENTS, INC.

Lacrimal probe, reusable
Primary Device ID00192896018686
NIH Device Record Keyfdc49f35-ae2f-460f-9dfb-061111070c23
Commercial Distribution StatusIn Commercial Distribution
Brand NameCRAWFORD LACRIMAL INTUBATION SET
Version Model Number16-2594
Catalog Number16-2594
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS100192896018686 [Primary]

FDA Product Code

HNLProbe, lachrymal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896018686]

Dry Heat Sterilization;Moist Heat or Steam 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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