ENDOLARYNGEAL MICRO KNOT PUSHER 1301-538

GUDID 00192896091610

ENDOLARYNGEAL KNOT PUSHER FORK SHAPED

SONTEC INSTRUMENTS, INC.

Rigid endoscopic biopsy needle, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable Suture knot pusher, reusable
Primary Device ID00192896091610
NIH Device Record Keyf4934fc3-a56f-4afb-b9fe-8b01a2e0698b
Commercial Distribution StatusIn Commercial Distribution
Brand NameENDOLARYNGEAL MICRO KNOT PUSHER
Version Model Number1301-538
Catalog Number1301-538
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

Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch
Length10 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896091610 [Primary]

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896091610]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-05-02
Device Publish Date2018-11-22

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