POOLE SUCTION TUBE 180-427

GUDID 00192896091542

POOLE SUCTION TUBE WITH VALVE

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 ID: 00192896091542
• NIH Device Record Key: a22085b1-e37d-481f-a0f2-62a7a1bb153d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POOLE SUCTION TUBE
• Version Model Number: 180-427
• Catalog Number: 180-427
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com
• Phone: +1(800)821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch
• Length: 10.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896091542 [Primary]

FDA Product Code

• JOL: CATHETER AND TIP, SUCTION

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896091542]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-12-24
• Device Publish Date: 2018-11-22

On-Brand Devices [POOLE SUCTION TUBE]

• 00192896091542: POOLE SUCTION TUBE WITH VALVE
• B0991804240: POOLE SUCTION TUBE CURVED
• B0991804220: POOLE SUCTION TUBE STRAIGHT
• 00192896114517: Poole Suction Tube Adolescent Curved