gudid Primary ID: 54-TA-2000

MD-Vue Lateral Access System (UDI 54-TA-2000)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MD-Vue Lateral Access System (Model/Catalog Number: 54-TA-2000) is a medical device manufactured by PRECISION SPINE, INC.. This product is indexed under FDA Product Code / Category Classification GAD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 54-TA-2000
Product Code / EMDN: GAD
Device Name: Table Arm
Database Sync Date: 2026-08-09 09:33:11

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of MD-Vue Lateral Access System?

The registered manufacturer of record for MD-Vue Lateral Access System is PRECISION SPINE, INC..

What is the Primary UDI-DI identifier for MD-Vue Lateral Access System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 54-TA-2000.

What classification code is assigned to this device?

This device is registered under product classification code GAD.

Similar Classification Devices (GAD)

Other Devices by PRECISION SPINE, INC.

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