EGRESS CANNULA SC94-0313

GUDID 00192896087804

EGRESS CANNULA WITH CONICAL OBTURATOR

SONTEC INSTRUMENTS, INC.

Suction cannula, reusable

• Primary Device ID: 00192896087804
• NIH Device Record Key: 3ab46c90-f9c3-4ab8-bff4-4070f61ad791
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EGRESS CANNULA
• Version Model Number: SC94-0313
• Catalog Number: SC94-0313
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 6 Inch
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896087804 [Primary]

FDA Product Code

• GEA: CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

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

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896087804]

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: 2018-10-22
• Device Publish Date: 2018-09-21

On-Brand Devices [EGRESS CANNULA]

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• 00192896087811: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896087804: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070608: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070592: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896070585: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896100428: EGRESS CANNULA WITH CONICAL OBTURATOR
• 00192896104730: Egress Cannula With Conical Obturator 8.1 Millimeter Inner Diameter
• 00192896110830: Egress Cannula With Conical Obturator 7.1 Millimeter Inner Diameter
• 00192896110984: Egress Cannula With Conical Obturator
• 00192896110977: Egress Cannula With Conical Obturator
• 00192896115552: Egress Cannula With Conical Obturator