MINI 3000 COMBINATION SET D-886.11.021

GUDID 00192896093126

MINI 3000 COMBINATION SET WITH LED

SONTEC INSTRUMENTS, INC.

Loupe
Primary Device ID00192896093126
NIH Device Record Key0f420636-7a83-403e-b192-b92b4c24e4e3
Commercial Distribution StatusIn Commercial Distribution
Brand NameMINI 3000 COMBINATION SET
Version Model NumberD-886.11.021
Catalog NumberD-886.11.021
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896093126 [Primary]

FDA Product Code

FSPLOUPE, DIAGNOSTIC/SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896093126]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-02-04
Device Publish Date2019-01-03

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