ROSS SUMP SUCKER

GUDID B09927003900

ROSS SUMP SUCKER ADULT

SONTEC INSTRUMENTS, INC.

Surgical/emergency suction cannula, non-illuminating, reusable

• Primary Device ID: B09927003900
• NIH Device Record Key: bf7e47eb-06a5-475b-8cf4-673f84fb9aa2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ROSS SUMP SUCKER
• Version Model Number: 2700-390
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM
• Phone: 8008217496
• Email: INFO@SONTECINSTRUMENTS.COM

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 7.5 Millimeter
• Length: 43 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896006072 [Primary]
HIBCC	B09927003900 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152400

FDA Product Code

• GCJ: Laparoscope, General & Plastic Surgery

Sterilization

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

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09927003900]

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: 2019-02-21
• Device Publish Date: 2018-08-21

On-Brand Devices [ROSS SUMP SUCKER]

• B09927003940: ROSS SUMP SUCKER INFANT
• B09927003920: ROSS SUMP SUCKER CHILD
• B09927003900: ROSS SUMP SUCKER ADULT