NeMus 1

GUDID 08056446900222

EMG/EP Amplifier with accessories

EB NEURO SPA

Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system Evoked-potential graphic recording system

• Primary Device ID: 08056446900222
• NIH Device Record Key: d475d34f-2d72-4ebf-b0fe-c8e231c83205
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NeMus 1
• Version Model Number: B9800066000
• Company DUNS: 339182263
• Company Name: EB NEURO SPA
• 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: false
• 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: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com
• Phone: +390554565111
• Email: info@ebneuro.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056446900222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K073415

FDA Product Code

• JXE: Device, Nerve Conduction Velocity Measurement

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-06-03
• Device Publish Date: 2019-05-24

On-Brand Devices [NeMus 1]

• 08056446900239: EMG/EP Amplifier
• 08056446900222: EMG/EP Amplifier with accessories