DISPERSIVE ELECTRODE CABLE A1254C

GUDID 00192896009196

RETURN ELECTRODE CORD

SONTEC INSTRUMENTS, INC.

Electrosurgical system generator

• Primary Device ID: 00192896009196
• NIH Device Record Key: 53c400e9-05d0-4a47-b1b3-996f31c61fa0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DISPERSIVE ELECTRODE CABLE
• Version Model Number: A1254C
• Catalog Number: A1254C
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• 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: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com
• Phone: 800-821-7496
• Email: info@sontecinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896009196 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K021817

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896009196]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-17
• Device Publish Date: 2018-08-15

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