GUDIDData
eudamed_udi Primary ID: 06420099000851

Medikro Primo (UDI 06420099000851)

Manufactured by Medikro Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medikro Primo - Primary ID 06420099000851

Device Regulatory Overview

The Medikro Primo (Model/Catalog Number: M914) is a medical device manufactured by Medikro Oy. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M914
Product Code / EMDN
Z12150101
Device Name
Medikro Primo
Database Sync Date
2026-08-09 17:48:54

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 Primo?

The registered manufacturer of record for Medikro Primo is Medikro Oy.

What is the Primary UDI-DI identifier for Medikro Primo?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06420099000851.

What classification code is assigned to this device?

This device is registered under product classification code Z12150101.

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