SONTEC SUCTION TUBE

GUDID B0991804430

SONTEC SUCTION TUBE WITH FINGER CONTROL

SONTEC INSTRUMENTS, INC.

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 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 IDB0991804430
NIH Device Record Key2c5aa573-07cb-4974-b54a-18cdaa6e8980
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC SUCTION TUBE
Version Model Number180-443
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
EmailINFO@SONTECINSTRUMENTS.COM
Phone8008217496
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

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Length14 Inch
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Length14 Inch
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Length14 Inch
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Length14 Inch
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Length14 Inch
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Length14 Inch
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Length14 Inch
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Device Size Text, specify0
Length14 Inch
Device Size Text, specify0
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Length14 Inch
Device Size Text, specify0
Device Size Text, specify0
Length14 Inch
Device Size Text, specify0
Device Size Text, specify0
Length14 Inch
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Device Size Text, specify0
Length14 Inch
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Device Size Text, specify0
Length14 Inch
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Length14 Inch
Device Size Text, specify0
Device Size Text, specify0
Length14 Inch
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Device Size Text, specify0
Length14 Inch
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Device Size Text, specify0
Length14 Inch
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Device Identifiers

Device Issuing AgencyDevice ID
GS100192896000056 [Primary]
HIBCCB0991804430 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B0991804430]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804430]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804430]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B0991804430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-04-25
Device Publish Date2018-08-31

On-Brand Devices [SONTEC SUCTION TUBE]

B0991804440SONTEC SUCTION TUBE WITH FINGER CONTROL
B0991804420SONTEC SUCTION TUBE WITH FINGER CONTROL
B0991804410SONTEC SUCTION TUBE WITH FINGER CONTROL
B0991804430SONTEC SUCTION TUBE WITH FINGER CONTROL
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