ANDREWS PYNCHON SUCTION TUBE 180-439

GUDID 00192896091665

ANDREWS PYNCHON SUCTION TIP CHROME

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 ID00192896091665
NIH Device Record Keya61c9c18-659e-4d0a-b8f3-40a9ccb0f8ea
Commercial Distribution StatusIn Commercial Distribution
Brand NameANDREWS PYNCHON SUCTION TUBE
Version Model Number180-439
Catalog Number180-439
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

Device Size Text, specify0
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0
Length9.5 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896091665 [Primary]

FDA Product Code

JOLCATHETER AND TIP, SUCTION

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896091665]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-24
Device Publish Date2018-11-22

On-Brand Devices [ANDREWS PYNCHON SUCTION TUBE]

00192896091665ANDREWS PYNCHON SUCTION TIP CHROME
B0991804370ANDREW PYNCHON SUCTION TUBE CHROME
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.