MARQUIS PROBE/EXPLORER 1103-319L

GUDID 00192896052741

MARQUIS PROBE/EXPLORER DOUBLE ENDED COLOR CODED TIPS #23

SONTEC INSTRUMENTS, INC.

Dental explorer
Primary Device ID00192896052741
NIH Device Record Keya6432f5c-7403-4338-aeb7-f270ade63a01
Commercial Distribution Discontinuation2019-03-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMARQUIS PROBE/EXPLORER
Version Model Number1103-319L
Catalog Number1103-319L
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
GS100192896052741 [Primary]

FDA Product Code

DZNINSTRUMENTS, DENTAL HAND

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896052741]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-03-25
Device Publish Date2018-09-24

On-Brand Devices [MARQUIS PROBE/EXPLORER]

00192896052741MARQUIS PROBE/EXPLORER DOUBLE ENDED COLOR CODED TIPS #23
00192896052734MARQUIS PROBE/EXPLORER #23

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