Curve 1.2 Dual Navigation Station 19901A/19901B

GUDID 04056481138011

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481138011
• NIH Device Record Key: 6beb46a4-7989-40be-a7f0-8f79ae4e6ffa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curve 1.2 Dual Navigation Station
• Version Model Number: 19901A
• Catalog Number: 19901A/19901B
• 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	04056481138011 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092467

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: 5
• Public Version Date: 2019-11-20
• Device Publish Date: 2018-01-04

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