PADDLE/CONDENSER 1102-REPFI3T

GUDID 00192896088023

PADDLE/CONDENSER #3T DOUBLE ENDED FLARED/FLAT BLADES LIGHT HANDLE TITANIUM

SONTEC INSTRUMENTS, INC.

Dental amalgam condenser, reusable

• Primary Device ID: 00192896088023
• NIH Device Record Key: 85088b42-3f3a-4edb-a577-57e6fa9ea89c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PADDLE/CONDENSER
• Version Model Number: 1102-REPFI3T
• Catalog Number: 1102-REPFI3T
• 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: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896088023 [Primary]

FDA Product Code

• EKG: CONDENSER, AMALGAM AND FOIL, OPERATIVE

Sterilization

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

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896088023]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-09-06
• Device Publish Date: 2018-09-17

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