Drill Guide Tube 3.2 X 150 mm 41839-30B

GUDID 04056481139520

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481139520
• NIH Device Record Key: a7fd829e-7a3b-4ae0-b82e-327f0e6afff6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Drill Guide Tube 3.2 X 150 mm
• Version Model Number: 41839-30B
• Catalog Number: 41839-30B
• 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: true
• Serial Number: false
• 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	04056481139520 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110204

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

[04056481139520]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-12
• Device Publish Date: 2018-01-26

On-Brand Devices [Drill Guide Tube 3.2 X 150 mm ]

• 04056481139520: 41839-30B
• 04056481003463: 41839-30A