SONTEC OPERATING LARYNGOSCOPE SUCTION TUBE 485-1341

GUDID 00192896080355

SONTEC OPERATING LARYNGOSCOPE SUCTION TUBE

SONTEC INSTRUMENTS, INC.

Tonsil suction cannula 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 ID00192896080355
NIH Device Record Key0ee6b2eb-bb26-40db-b116-307a0496ddd8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC OPERATING LARYNGOSCOPE SUCTION TUBE
Version Model Number485-1341
Catalog Number485-1341
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

Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch
Length5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896080355 [Primary]

FDA Product Code

JZFTUBE, EAR SUCTION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896080355]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-20

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