ANDREWS PYNCHON SUCTION TUBE

GUDID B0991804370

ANDREW PYNCHON SUCTION TUBE CHROME

SONTEC INSTRUMENTS, INC.

Suction cannula, reusable 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: B0991804370
• NIH Device Record Key: 1be029e8-0785-4cf2-9621-432896d64e55
• Commercial Distribution Discontinuation: 2018-06-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ANDREWS PYNCHON SUCTION TUBE
• Version Model Number: 180-437
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 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: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch
• Length: 8.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B0991804370 [Primary]

FDA Product Code

• JOL: Catheter And Tip, Suction

Sterilization

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

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B0991804370]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-06-22
• Device Publish Date: 2017-09-30

On-Brand Devices [ANDREWS PYNCHON SUCTION TUBE]

• 00192896091665: ANDREWS PYNCHON SUCTION TIP CHROME
• B0991804370: ANDREW PYNCHON SUCTION TUBE CHROME