Horizon 3.0 Interface Unit

GUDID 05060229532732

THE MAGSTIM COMPANY LIMITED

Magnetic neural stimulation system

• Primary Device ID: 05060229532732
• NIH Device Record Key: 8e1747d1-6b74-4de2-9ddf-4f4475105434
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Horizon 3.0 Interface Unit
• Version Model Number: 5790-00
• Company DUNS: 500375274
• Company Name: THE MAGSTIM COMPANY LIMITED
• 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: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com
• Phone: +441994241111
• Email: salesoperations@magstim.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060229532732 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211389

FDA Product Code

• OBP: Transcranial Magnetic Stimulator

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: 2021-12-29
• Device Publish Date: 2021-12-21

On-Brand Devices [Horizon 3.0 Interface Unit ]

• 05060229532732: 5790-00
• 05060229533005: Horizon 3.0 Interface Unit