Dorsey Grasping Forceps

GUDID 00192896110571

Dorsey Grasping Forceps Fenestrated Single Action Jaw 5 Millimeter Diameter Tube

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 00192896110571
• NIH Device Record Key: acfde461-7e2b-4b01-b5bb-4f5db2ee1ccc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dorsey Grasping Forceps
• Version Model Number: 2901-217
• 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

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896110571 [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

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896110571]

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: 2021-07-20
• Device Publish Date: 2021-07-12

On-Brand Devices [Dorsey Grasping Forceps]

• 00192896094611: DORSEY GRASPING FORCEPS DOUBLE ACTION FENESTRATED JAW
• 00192896110588: Dorsey Grasping Forceps Fenestrated Single Action Jaw Diameter 5 Millimeter Tube
• 00192896110571: Dorsey Grasping Forceps Fenestrated Single Action Jaw 5 Millimeter Diameter Tube