SCOVILLE NERVE ROOT RETRACTOR 412-643A

GUDID 00192896036024

SCOVILLE NERVE ROOT RETRACTOR STRAIGHT SHAFT

SONTEC INSTRUMENTS, INC.

Nerve/vessel retractor

• Primary Device ID: 00192896036024
• NIH Device Record Key: 9a1eb934-9c5d-4933-bcba-0e45be9e9da2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCOVILLE NERVE ROOT RETRACTOR
• Version Model Number: 412-643A
• Catalog Number: 412-643A
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00192896036024 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00192896036024]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-12-21
• Device Publish Date: 2018-09-18

On-Brand Devices [SCOVILLE NERVE ROOT RETRACTOR]

• 00192896079120: SCOVILLE NERVE ROOT RETRACTOR FULL CURVED TIP
• 00192896036031: SCOVILLE NERVE ROOT RETRACTOR BAYONET SHAFT
• 00192896036024: SCOVILLE NERVE ROOT RETRACTOR STRAIGHT SHAFT