SONTEC LARYNGOSCOPE SUCTION TUBE 485-1342

GUDID 00192896043626

SONTEC LARYNGOSCOPE SUCTION TUBE

SONTEC INSTRUMENTS, INC.

Bone clamp traction bar Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable
Primary Device ID00192896043626
NIH Device Record Keyfe23b76a-25bb-41a8-9f74-bcb693c8cc12
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC LARYNGOSCOPE SUCTION TUBE
Version Model Number485-1342
Catalog Number485-1342
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

Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch
Length3.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896043626 [Primary]

FDA Product Code

JZFTUBE, EAR SUCTION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896043626]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-25
Device Publish Date2018-09-24

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