Registr. Matrix Imri Ge Headholder 19202B

GUDID 04056481004460

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481004460
• NIH Device Record Key: dce94a74-7826-4ec3-a764-c35202233bff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Registr. Matrix Imri Ge Headholder
• Version Model Number: 19202B
• Catalog Number: 19202B
• Company DUNS: 314482980
• Company Name: Brainlab AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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	04056481004460 [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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-15

On-Brand Devices [Registr. Matrix Imri Ge Headholder]

• 04056481131920: 19202C
• 04056481004491: 19202-01C
• 04056481004477: 19202-20C
• 04056481004460: 19202B