Disp Self-Drilling Screw 1.5X6Mm Kls 52170

GUDID 04056481006013

Brainlab AG

Robotic surgical navigation system

• Primary Device ID: 04056481006013
• NIH Device Record Key: 7d84a5c7-b756-4604-8327-24d84c757709
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Disp Self-Drilling Screw 1.5X6Mm Kls
• Version Model Number: 52170
• Catalog Number: 52170
• 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: true
• 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
• 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	04056481006013 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092467

FDA Product Code

• HAW: Neurological Stereotaxic Instrument

Sterilization

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

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

Moist Heat or Steam Sterilization

[04056481006013]

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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• 04056481125967 - Patient Mask Set: 2025-03-18
• 04056481142698 - Frameless SRS MASK SET CRANIAL: 2025-03-18
• 04056481142704 - Frameless SRS MASK SET EXTENDED: 2025-03-18
• 04056481145620 - Alignment Reduction Tube Cranial 8.0 mm / 10.0 mm: 2025-03-04
• 04056481145637 - Alignment Guide Tube Cranial 4.9 mm / 8.0 mm: 2025-03-04
• 04056481145903 - Alignment Bone Anchor Cranial 2.1 mm / 4.9 mm: 2025-03-04