VICKERS K-WIRE PIN BENDER 1103-178A

GUDID 00192896088535

VICKERS K-WIRE PIN BENDER BLACK COATED

SONTEC INSTRUMENTS, INC.

Manual orthopaedic bender, reusable

• Primary Device ID: 00192896088535
• NIH Device Record Key: 5efdb859-d902-4ab3-9d52-caabbb5f1f47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VICKERS K-WIRE PIN BENDER
• Version Model Number: 1103-178A
• Catalog Number: 1103-178A
• 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	00192896088535 [Primary]

FDA Product Code

• GFC: DRIVER, SURGICAL, PIN

Sterilization

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

[00192896088535]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-10
• Device Publish Date: 2018-09-11

On-Brand Devices [VICKERS K-WIRE PIN BENDER]

• 00192896088542: VICKERS K-WIRE PIN BENDER BLACK COATED
• 00192896088535: VICKERS K-WIRE PIN BENDER BLACK COATED