Stem Verification Tool Hip Ct 52872B

GUDID 04056481001902

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481001902
• NIH Device Record Key: 5b35b379-24ef-4348-8b08-84a6c8cebd2c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stem Verification Tool Hip Ct
• Version Model Number: 52872B
• Catalog Number: 52872B
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481001902 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K083483

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

[04056481001902]

Moist Heat or Steam Sterilization

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

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• 04056481146238 - PATIENT REFERENCE ARRAY SPINE & TRAUMA: 2024-11-22
• 04056481146603 - ADAPTER SHORT FOR PATIENT REFERENCE CLAMP: 2024-11-22
• 04056481146610 - ADAPTER X-PRESS FOR PATIENT REFERENCE ARRAY: 2024-11-22
• 04056481143916 - Spine Planning: 2024-11-13
• 04056481144654 - Viewer 5.4: 2024-11-13
• 04056481143527 - DICOM Proxy: 2024-11-01