Fluorostar 55735A

GUDID 04056481001629

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481001629
• NIH Device Record Key: b5c3c29a-7fba-44f4-9016-e03afa799e92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fluorostar
• Version Model Number: 55735A
• Catalog Number: 55735A
• Company DUNS: 314482980
• Company Name: Brainlab 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: 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: +49899915680
• Email: contact@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481001629 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070106

FDA Product Code

• HAW: Neurological Stereotaxic Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-11
• Device Publish Date: 2016-09-15

Devices Manufactured by Brainlab AG

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• 04056481144906 - Spine &Trauma Navigation: 2024-11-22
• 04056481146238 - PATIENT REFERENCE ARRAY SPINE & TRAUMA: 2024-11-22
• 04056481146603 - ADAPTER SHORT FOR PATIENT REFERENCE CLAMP: 2024-11-22
• 04056481146610 - ADAPTER X-PRESS FOR PATIENT REFERENCE ARRAY: 2024-11-22
• 04056481143916 - Spine Planning: 2024-11-13
• 04056481144654 - Viewer 5.4: 2024-11-13
• 04056481143527 - DICOM Proxy: 2024-11-01