HOUSE BARON SUCTION TUBE

GUDID B099412729B0

HOUSE BARON SUCTION TUBE

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 Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable

• Primary Device ID: B099412729B0
• NIH Device Record Key: 74956411-2b83-443d-9167-763e69a2c487
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOUSE BARON SUCTION TUBE
• Version Model Number: 412-729B
• 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: 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: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0
• Length: 7 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896011199 [Primary]
HIBCC	B099412729B0 [Previous]

FDA Product Code

• JOL: Catheter And Tip, Suction

Sterilization

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

[B099412729B0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B099412729B0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B099412729B0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B099412729B0]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-04-24
• Device Publish Date: 2018-08-21

On-Brand Devices [HOUSE BARON SUCTION TUBE]

• B099412729B0: HOUSE BARON SUCTION TUBE
• B0994127280: HOUSE BARON SUCTION TUBE
• B0994127290: HOUSE BARON SUCTION TUBE
• B099412728B0: HOUSE BARON SUCTION TUBE WITH MULTI PORT
• B099412727B0: HOUSE BARON SUCTION TUBE
• B099412727A0: HOUSE BARON SUCTION TUBE
• 00192896108615: House Baron Suction Tube 5 French With Multi Port
• 00192896117273: House Baron Suction Tube With Multi-Port
• 00192896117266: House Baron Suction Tube With Multi-Port
• 00192896117259: House Baron Suction Tube With Multi-Port