Home GUDID 07630542735554 NextAR Spine Platform
Primary DI 07630542735554
Brand NextAR Spine Platform
Company Medacta International SA
Model 03.57.10.0231
Device description NextAR Spine MC Cortical Tap Cannulated – 5.5mm
Published 2024-12-03
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name SBF Orthopedic Augmented Reality
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class SBF Orthopedic Augmented Reality Neurology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07630542735554 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630542735554 07630542735554 7630542735554
GMDN Terms# Term, Definition table Term Definition Optical surgical navigation/tracking system A mobile assembly of electrically-powered devices intended to provide a physician with optical tools to track manual surgical instruments and locate anatomical structures; it may be intended to overlay pre-acquired radiological images or real-time data [e.g., ultrasound (US)] for surgical navigation, and be capable of creating digital 3-D patient models. It consists of a workstation with controls/display, position/movement tracking cameras (e.g., infrared), adaptors, and sensors/spatial markers designed to be attached to the patient and instruments. It is used for multiple surgical procedures (e.g., craniotomy, tumour resection) in various fields [e.g., ENT, neurosurgery, CMF surgery].
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 488227125 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 07630040738767 Surgical Manual Instrument 01.22.10.0051 2026-09-21 07630345706584 M-Vizion Femoral Revision System Extension 01.22.10.0781 2026-09-21 07630345706591 M-Vizion Femoral Revision System Extension 01.22.10.0782 2026-09-21 07630345706607 M-Vizion Femoral Revision System Extension 01.22.10.0783 2026-09-21 07630345706614 M-Vizion Femoral Revision System Extension 01.22.10.0784 2026-09-21 07630345706621 M-Vizion Femoral Revision System Extension 01.22.10.0785 2026-09-21 07630345706638 M-Vizion Femoral Revision System Extension 01.22.10.0786 2026-09-21 07630345706645 M-Vizion Femoral Revision System Extension 01.22.10.0787 2026-09-21 07630345706652 M-Vizion Femoral Revision System Extension 01.22.10.0788 2026-09-21 07630345706669 M-Vizion Femoral Revision System Extension 01.22.10.0789 2026-09-21 07630345706676 M-Vizion Femoral Revision System Extension 01.22.10.0790 2026-09-21 07630345706683 M-Vizion Femoral Revision System Extension 01.22.10.0791 2026-09-21 07630345706690 M-Vizion Femoral Revision System Extension 01.22.10.0792 2026-09-21 07630345706706 M-Vizion Femoral Revision System Extension 01.22.10.0793 2026-09-21 07630345706713 M-Vizion Femoral Revision System Extension 01.22.10.0794 2026-09-21 07630345706720 M-Vizion Femoral Revision System Extension 01.22.10.0795 2026-09-21 07630542702112 Surgical Manual Instrument 01.22.10.0174 2026-09-21 07630542723162 M-Vizion Femoral Revision System Extension 01.22.10.0402 2026-09-21 07630542728563 M-Vizion Femoral Revision System Extension 01.22.10.0779 2026-09-21 07630542728570 M-Vizion Femoral Revision System Extension 01.22.10.0780 2026-09-21
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