PIN BENDER 1103-201

GUDID 00192896082755

PIN BENDER DOUBLE ENDED TIPS

SONTEC INSTRUMENTS, INC.

Orthopaedic implant calibration pin

• Primary Device ID: 00192896082755
• NIH Device Record Key: ddcb02ee-e2c3-40c8-ae54-5ee64ffa5fec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PIN BENDER
• Version Model Number: 1103-201
• Catalog Number: 1103-201
• 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
• Phone: +1(800) 821-7496
• Email: info@sontecinstruments.com

Device Dimensions

• Length: 5 Inch
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch
• Device Size Text, specify: 0
• Length: 5 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896082755 [Primary]

FDA Product Code

• GFC: Driver, Surgical, Pin
• HWX: TAP, BONE

Sterilization

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

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00192896082755]

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: 2018-10-22
• Device Publish Date: 2018-09-21

On-Brand Devices [PIN BENDER]

• 00192896082755: PIN BENDER DOUBLE ENDED TIPS
• 00192896053984: PIN BENDER DOUBLE ENDED TIPS
• 00192896053960: PIN BENDER DOUBLE ENDED TIPS