JACKSON TRACHEAL RETRACTOR 502-399

GUDID 00192896044210

JACKSON TRACHEAL RETRACTOR

SONTEC INSTRUMENTS, INC.

Tracheal hook
Primary Device ID00192896044210
NIH Device Record Keyb5c372cb-5d07-4e0e-ac2f-c0aa4257ffb8
Commercial Distribution StatusIn Commercial Distribution
Brand NameJACKSON TRACHEAL RETRACTOR
Version Model Number502-399
Catalog Number502-399
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
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch
Length7 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896044210 [Primary]

FDA Product Code

KALRETRACTOR, ENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896044210]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-15
Device Publish Date2018-09-14

On-Brand Devices [JACKSON TRACHEAL RETRACTOR]

00192896092327JACKSON TRACHEAL RETRACTOR BLUE ELECTRO COATED
00192896044210JACKSON TRACHEAL RETRACTOR
00192896118034Jackson Tracheal Retractor Double End 2 Sharp Prongs Titanium

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