Periodontal Knife

GUDID 00192896102569

Goldman-Fox Periodontal Knife #8 Double Ended "Spear" Offset Blades

SONTEC INSTRUMENTS, INC.

Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife Periodontal knife

• Primary Device ID: 00192896102569
• NIH Device Record Key: 7909b8cb-f188-42ce-88d2-4859f94f3fac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Periodontal Knife
• Version Model Number: 1102-KGF8
• Company DUNS: 040729840
• Company Name: SONTEC INSTRUMENTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896102569 [Primary]

FDA Product Code

• EMF: KNIFE, SURGICAL

Sterilization

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

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896102569]

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: 2020-06-23
• Device Publish Date: 2020-06-15

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