SCOVILLE NERVE ROOT RETRACTOR 412-644C

GUDID 00192896079120

SCOVILLE NERVE ROOT RETRACTOR FULL CURVED TIP

SONTEC INSTRUMENTS, INC.

Nerve/vessel retractor

• Primary Device ID: 00192896079120
• NIH Device Record Key: e7477b0a-c2dc-4339-9a8c-3a79def80d89
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCOVILLE NERVE ROOT RETRACTOR
• Version Model Number: 412-644C
• Catalog Number: 412-644C
• 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	00192896079120 [Primary]

FDA Product Code

• FGN: RETRACTOR, NON-SELF-RETAINING

Sterilization

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

[00192896079120]

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: 2018-09-20

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