eudamed_udi
Primary ID: 06420099000837
Medikro Pro (UDI 06420099000837)
Manufactured by Medikro Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medikro Pro - Primary ID 06420099000837
Device Regulatory Overview
The Medikro Pro (Model/Catalog Number: M915) 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
- M915
- Product Code / EMDN
- Z12150101
- Device Name
- Medikro Pro
- Database Sync Date
- 2026-08-09 18:16:48
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Medikro Pro?
The registered manufacturer of record for Medikro Pro is Medikro Oy.
What is the Primary UDI-DI identifier for Medikro Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06420099000837.
What classification code is assigned to this device?
This device is registered under product classification code Z12150101.
Similar Classification Devices (Z12150101)
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