Poole Suction Tube

GUDID 00192896114517

Poole Suction Tube Adolescent Curved

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

• Primary Device ID: 00192896114517
• NIH Device Record Key: 33639102-eac9-4f08-9a85-dad36f74cfea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Poole Suction Tube
• Version Model Number: 180-420L
• 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: true
• 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

Device Dimensions

• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0
• Length: 8.25 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896114517 [Primary]

FDA Product Code

• JOL: CATHETER AND TIP, SUCTION

Sterilization

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

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896114517]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-06
• Device Publish Date: 2023-02-24

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