Phantom Pointer 40900-3A

GUDID 04056481004088

Brainlab AG

Head/neck procedure positioner

• Primary Device ID: 04056481004088
• NIH Device Record Key: ba3f0bbe-e7cd-41ce-9d5f-7f9dd8fbc17d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phantom Pointer
• Version Model Number: 40900-3A
• Catalog Number: 40900-3A
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +49899915680
• Email: contact@brainlab.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481004088 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K934657

FDA Product Code

• IYE: Accelerator, Linear, Medical

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 [Phantom Pointer]

• 04056481004095: 40900-1
• 04056481004088: 40900-3A