THORACIC SUCTION TUBE 180-4291

GUDID 00192896088115

THORACIC SUCTION TUBE WITH PYNCHON HANDLE WITHOUT HOLE STRAIGHT

SONTEC INSTRUMENTS, INC.

Suction cannula, 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 ID00192896088115
NIH Device Record Keyf1346a5a-3c78-4374-86d4-97eff74cab61
Commercial Distribution StatusIn Commercial Distribution
Brand NameTHORACIC SUCTION TUBE
Version Model Number180-4291
Catalog Number180-4291
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

Phone800-821-7496
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

Device Size Text, specify0
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0
Length17.25 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896088115 [Primary]

FDA Product Code

JOLCatheter And Tip, Suction

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896088115]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-17
Device Publish Date2018-08-15

On-Brand Devices [THORACIC SUCTION TUBE]

00192896088115THORACIC SUCTION TUBE WITH PYNCHON HANDLE WITHOUT HOLE STRAIGHT
00192896000490THORACIC SUCTION TUBE WITH PYNCHON HANDLE WITHOUT HOLE STRAIGHT
B0991804310THORACIC SUCTION TUBE WITH PYNCHON HANDLE STRAIGHT
B099180429F0THORACIC SUCTION TUBE WITH FLAT HANDLE STRAIGHT
B099180429CB0THORACIC SUCTION TUBE WITH PYNCHON HANDLE AND BASKET ANGLED
B099180429C0THORACIC SUCTION TUBE WITH PYNCHON HANDLE CURVED
B099180429B0THORACIC SUCTION TUBE WITH PYNCHON HANDLE AND BASKET STRAIGHT
B0991804290THORACIC SUCTION TUBE WITH PYNCHON HANDLE STRAIGHT
B099180431C0THORACIC SUCTION TUBE WITH PYNCHON HANDLE ANGLED
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