gudid Primary ID: ME-CHECK 4

ME-CHECK 4 (UDI ME-CHECK 4)

Manufactured by ESPANSIONE MARKETING SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ME-CHECK 4 (Model/Catalog Number: ME-CHECK 4) is a medical device manufactured by ESPANSIONE MARKETING SPA. This product is indexed under FDA Product Code / Category Classification PJZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ME-CHECK 4
Product Code / EMDN: PJZ
Device Name
Database Sync Date: 2026-08-09 09:04:29

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 ME-CHECK 4?

The registered manufacturer of record for ME-CHECK 4 is ESPANSIONE MARKETING SPA.

What is the Primary UDI-DI identifier for ME-CHECK 4?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ME-CHECK 4.

What classification code is assigned to this device?

This device is registered under product classification code PJZ.

Similar Classification Devices (PJZ)

Other Devices by ESPANSIONE MARKETING SPA

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