Surgical Base System

GUDID 04260583190017

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04260583190017
• NIH Device Record Key: 95820347-fc60-44b6-b26c-bfa66966585b
• Commercial Distribution Discontinuation: 2019-12-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Surgical Base System
• Version Model Number: 20100131
• Company DUNS: 314482980
• Company Name: Brainlab AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	04260583190017 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183605

FDA Product Code

• OLO: Orthopedic 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: 2
• Public Version Date: 2019-12-12
• Device Publish Date: 2019-09-05

Devices Manufactured by Brainlab AG

• 04056481143916 - Spine Planning: 2024-11-13
• 04056481144654 - Viewer 5.4: 2024-11-13
• 04056481143527 - DICOM Proxy: 2024-11-01
• 04056481144913 - CRANIAL 4PI STEREOTACTIC MASK (5 PCS.): 2024-07-26
• 04056481144920 - CRANIAL 4PI STEREOTACTIC MASK (1 PC.): 2024-07-26
• 04056481144937 - CRANIAL 4PI BASIC MASK (5 PCS.): 2024-07-26
• 04056481144944 - CRANIAL 4PI BASIC MASK (1 PC.): 2024-07-26
• 04056481144951 - CRANIAL 4PI OPEN FACE MASK (5 PCS.): 2024-07-26