WIRE/PIN CUTTER 1103-102

GUDID 00192896051430

WIRE/PIN CUTTER DOUBLE ACTION ANGLED TUNGSTEN CARBIDE BLADES

SONTEC INSTRUMENTS, INC.

Wire cutter

• Primary Device ID: 00192896051430
• NIH Device Record Key: 3845f756-cf61-4b65-a317-f1bbaa1b46c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WIRE/PIN CUTTER
• Version Model Number: 1103-102
• Catalog Number: 1103-102
• 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
• 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: 8.75 Inch
• Length: 8.75 Inch
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 8.75 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896051430 [Primary]

FDA Product Code

• HXZ: CUTTER, WIRE

Sterilization

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

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[00192896051430]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-09-17
• Device Publish Date: 2018-09-10

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• 00192896047983: WIRE/PIN CUTTER DOUBLE ACTION TUNGSTEN CARBIDE UP-ANGLE BLADES
• 00192896047976: WIRE/PIN CUTTER DOUBLE ACTION TUNGSTEN CARBIDE ANGLED TO SIDE BLADES
• 00192896097179: WIRE/PIN CUTTER DOUBLE ACTION ANGLED TUNGSTEN CARBIDE BLADE
• 00192896109933: Wire/Pin Cutter Double Action Tungsten Carbide Angled Up Quantum
• 00192896110519: Wire/Pin Cutter Double Action Tungsten Carbide Angled Up Quantum