INTRACAPULAR MANIPULATING WAND 12-1405

GUDID 00192896072503

INTRACAPULAR MANIPULATING WAND STRAIGHT TIP STAINLESS STEEL

SONTEC INSTRUMENTS, INC.

Eye spud/needle
Primary Device ID00192896072503
NIH Device Record Keya75151fa-feee-4201-b306-3b4bfb35c366
Commercial Distribution StatusIn Commercial Distribution
Brand NameINTRACAPULAR MANIPULATING WAND
Version Model Number12-1405
Catalog Number12-1405
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
GS100192896072503 [Primary]

FDA Product Code

HNASpud, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072503]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-19

On-Brand Devices [INTRACAPULAR MANIPULATING WAND]

00192896072541INTRACAPULAR MANIPULATING WAND STRAIGHT TIP TITANIUM
00192896072503INTRACAPULAR MANIPULATING WAND STRAIGHT TIP STAINLESS STEEL
00192896013124INTRACAPULAR MANIPULATING WAND ANGLED TIP TITANIUM

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