Alignment Trocar Spine 3.2 56332-32

GUDID 04056481141332

Brainlab AG

Electromagnetic/optical surgical navigation device tracking system

• Primary Device ID: 04056481141332
• NIH Device Record Key: 83154299-504d-401c-a9b5-5c45b83632e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alignment Trocar Spine 3.2
• Version Model Number: 56332-32
• Catalog Number: 56332-32
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04056481141332 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202320

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

[04056481141332]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-09-18
• Device Publish Date: 2022-12-27

Devices Manufactured by Brainlab AG

• 04056481145514 - Z-touch Laser Registration Pointer: 2025-02-21 The Z-touch Laser Registration Pointer is a battery powered wireless laser pointer for quick and accurate patient registration w
• 04056481144906 - Spine &Trauma Navigation: 2024-11-22
• 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