WIRE END CUTTER 1103-100Q

GUDID 00192896082571

WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE TIPS

SONTEC INSTRUMENTS, INC.

Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter Wire cutter
Primary Device ID00192896082571
NIH Device Record Keyac7920a3-1803-4a7e-a26d-a343e051399f
Commercial Distribution StatusIn Commercial Distribution
Brand NameWIRE END CUTTER
Version Model Number1103-100Q
Catalog Number1103-100Q
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

Device Dimensions

Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch
Device Size Text, specify0
Length8.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896082571 [Primary]

FDA Product Code

HXZCUTTER, WIRE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[00192896082571]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-06-03
Device Publish Date2018-09-21

On-Brand Devices [WIRE END CUTTER]

00192896082595WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE BLADES
00192896082571WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE TIPS
00192896051522WIRE SIDE CUTTER TUNGSTEN CARBIDE BLADES
00192896051515WIRE END CUTTER TUNGSTEN CARBIDE BLADES
00192896051485WIRE END CUTTER DOUBLE SPRING ACTION TUNGSTEN CARBIDE BLADES
00192896051416WIRE END CUTTER DOUBLE ACTION TUNGSTEN CARBIDE BLADES
00192896105195WIRE END CUTTER DOUBLE SPRING ACTION TUNGSTEN CARBIDE CUTS WIRE UP TO 1.5 MILLIMETERS 6.25 INCHE

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.