Tube Shaft

GUDID 00192896103627

Tube Shaft Insulated With Luer Lock

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

• Primary Device ID: 00192896103627
• NIH Device Record Key: 2c5d5cbf-b21f-4aef-8aa9-207a050e2943
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tube Shaft
• Version Model Number: 2901-103L
• 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

Device Dimensions

• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0
• Length: 450 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896103627 [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

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896103627]

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: 2020-07-31
• Device Publish Date: 2020-07-23

On-Brand Devices [Tube Shaft]

• 00192896092341: TUBE SHAFT WITH LUER LOCK INSULATED CYLINDRICAL TUBE
• 00192896093430: TUBE SHAFT WITH LUER LOCK INSULATED
• 00192896103627: Tube Shaft Insulated With Luer Lock
• 00192896110472: Tube Shaft Diameter 5 Millimeter, Insulated Without Luer Lock
• 00192896110465: Tube Shaft Diameter 5 Millimeter, Insulated Without Luer Lock
• 00192896111912: Tube Shaft/Insulated Cylindrical Without Luer Lock