Apollo Light TMS Therapy System

GUDID 04260526050101

MAG & More GmbH

Magnetic neural stimulation system

• Primary Device ID: 04260526050101
• NIH Device Record Key: 5d92b7f2-f420-479c-b465-470561d0fd0e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Apollo Light TMS Therapy System
• Version Model Number: 918010
• Company DUNS: 328246368
• Company Name: MAG & More GmbH
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260526050101 [Primary]

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: 2024-08-29
• Device Publish Date: 2024-08-21

Devices Manufactured by MAG & More GmbH

• 04260526050101 - Apollo Light TMS Therapy System: 2024-08-29
• 04260526050101 - Apollo Light TMS Therapy System: 2024-08-29
• 04260526050019 - Apollo TMS Therapy System: 2023-06-01