Power Cut Preparation Scissors 2901-303L

GUDID 00192896115088

Power Cut Preparation Scissors Curved Double Action Jaw Insert For 5 Millimeter Diameter Tube Shaft

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00192896115088
• NIH Device Record Key: ebffa59e-5eed-4480-9990-d7a2437ffc54
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Power Cut Preparation Scissors
• Version Model Number: 2901-303L
• Catalog Number: 2901-303L
• 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: true
• 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

Device Dimensions

• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter
• Length: 450 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896115088 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102921

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896115088]

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: 2023-07-03
• Device Publish Date: 2023-06-23

On-Brand Devices [Power Cut Preparation Scissors]

• B09929013030: POWER CUT PREPARATION SCISSORS CURVED DOUBLE-ACTION JAW
• 00192896115088: Power Cut Preparation Scissors Curved Double Action Jaw Insert For 5 Millimeter Diameter Tube Sh