HighSurg 30

GUDID ENOU33600

Surgical motor system

Nouvag AG

Line-powered surgical power tool system motor Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered Surgical power tool system control unit, line-powered

• Primary Device ID: ENOU33600
• NIH Device Record Key: 51b0a618-f645-481f-b8ce-078a5b3ed9e5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HighSurg 30
• Version Model Number: 3360
• Company DUNS: 480610476
• Company Name: Nouvag AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com
• Phone: +41718466600
• Email: info@nouvag.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ENOU33600 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042434

FDA Product Code

• HBC: Motor, Drill, Electric

Sterilization

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

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

[ENOU33600]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-01-13

On-Brand Devices [HighSurg 30]

• ENOU33900: Surgical motor system
• ENOU33650: Surgical motor system
• ENOU33600: Surgical motor system