Gerald Bipolar Forceps

GUDID 00192896109223

Gerald Bipolar Forceps Fine Straight

SONTEC INSTRUMENTS, INC.

Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable Endoscopic electrosurgical handpiece/electrode, bipolar, reusable

• Primary Device ID: 00192896109223
• NIH Device Record Key: 2b0d4afb-0f0d-41f6-99f9-900e0ca6016f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Gerald Bipolar Forceps
• Version Model Number: 412-399
• 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: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch
• Length: 7.25 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896109223 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101080

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896109223]

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: 2021-05-14
• Device Publish Date: 2021-05-06

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