MULDON LACRIMAL DILATOR 16-2500

GUDID 00192896018518

MULDON LACRIMAL DILATOR SINGLE ENDED

SONTEC INSTRUMENTS, INC.

Lacrimal dilator, reusable
Primary Device ID00192896018518
NIH Device Record Keyfd3c1184-ce4d-4928-a5a3-17186c08045d
Commercial Distribution StatusIn Commercial Distribution
Brand NameMULDON LACRIMAL DILATOR
Version Model Number16-2500
Catalog Number16-2500
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 Identifiers

Device Issuing AgencyDevice ID
GS100192896018518 [Primary]

FDA Product Code

HNWDilator, lachrymal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896018518]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-18
Device Publish Date2018-09-17

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