PIN BENDER 1106-196

GUDID 00192896053960

PIN BENDER DOUBLE ENDED TIPS

SONTEC INSTRUMENTS, INC.

Manual orthopaedic bender, reusable

• Primary Device ID: 00192896053960
• NIH Device Record Key: a2d8380a-3c8e-4351-b9a1-9d383d664fd7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PIN BENDER
• Version Model Number: 1106-196
• Catalog Number: 1106-196
• 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

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00192896053960 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument
• HXP: Instrument, Bending Or Contouring

Sterilization

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

[00192896053960]

Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-27
• Device Publish Date: 2018-09-11

On-Brand Devices [PIN BENDER]

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