gudid Primary ID: V800

MARTIN LEWIS G.C. SYSTEM (UDI V800)

Manufactured by Healthlink

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MARTIN LEWIS G.C. SYSTEM (Model/Catalog Number: V800) is a medical device manufactured by Healthlink. This product is indexed under FDA Product Code / Category Classification JTY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: V800
Product Code / EMDN: JTY
Device Name: MARTIN LEWIS G.C. SYSTEM
Database Sync Date: 2026-08-09 09:14:44

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 MARTIN LEWIS G.C. SYSTEM?

The registered manufacturer of record for MARTIN LEWIS G.C. SYSTEM is Healthlink.

What is the Primary UDI-DI identifier for MARTIN LEWIS G.C. SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V800.

What classification code is assigned to this device?

This device is registered under product classification code JTY.

Similar Classification Devices (JTY)

Other Devices by Healthlink

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