Hook Scissors 2901-307

GUDID 00192896120181

Hook Scissors Single Action Jaws

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00192896120181
• NIH Device Record Key: 6101beb9-103e-4b8d-bfae-7140d3852b65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hook Scissors
• Version Model Number: 2901-307
• Catalog Number: 2901-307
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 360 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896120181 [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

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

[00192896120181]

Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-23
• Device Publish Date: 2024-10-15

On-Brand Devices [Hook Scissors]

• B0992901314S0: HOOK SCISSORS SINGLE-ACTION JAW
• B0992901314L0: HOOK SCISSORS SINGLE-ACTION JAW
• B09929013140: HOOK SCISSORS SINGLE-ACTION JAW
• 00192896100268: HOOK SCISSORS WITH OVERLOAD CONE ANGLED RIGHT
• 00192896098336: HOOK SCISSORS WITH OVERLOAD CONE STRAIGHT TIP
• 00192896115095: Hook Scissors Single Action Jaw Insert For 5 Millimeter Diameter Tube Shaft
• 00192896120181: Hook Scissors Single Action Jaws