GUDIDData
eudamed_udi Primary ID: 06420099001476

Medikro Spirometry Software (UDI 06420099001476)

Manufactured by Medikro Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medikro Spirometry Software - Primary ID 06420099001476

Device Regulatory Overview

The Medikro Spirometry Software (Model/Catalog Number: M9831) is a medical device manufactured by Medikro Oy. This product is indexed under FDA Product Code / Category Classification Z12150192 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M9831
Product Code / EMDN
Z12150192
Device Name
Medikro Spirometry Software
Database Sync Date
2026-08-09 17:32:44

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 Medikro Spirometry Software?

The registered manufacturer of record for Medikro Spirometry Software is Medikro Oy.

What is the Primary UDI-DI identifier for Medikro Spirometry Software?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06420099001476.

What classification code is assigned to this device?

This device is registered under product classification code Z12150192.

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