Curve™ 19900

GUDID 04056481006372

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481006372
• NIH Device Record Key: 815e2296-1960-4e25-bb44-7ea52bc0b154
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curve™
• Version Model Number: 19900
• Catalog Number: 19900
• 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: 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: +49899915680
• Email: contact@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481006372 [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: 4
• Public Version Date: 2019-11-20
• Device Publish Date: 2016-09-15

On-Brand Devices [Curve™]

• 04056481006372: 19900
• 04056481006365: 19901
• 04056481006358: 19905