gudid
Primary ID: M9488
M915, Medikro Pro (UDI M9488)
Manufactured by Medikro Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for M915, Medikro Pro - Primary ID M9488
Device Regulatory Overview
The M915, Medikro Pro (Model/Catalog Number: M9488) is a medical device manufactured by Medikro Oy. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M9488
- Product Code / EMDN
- BZG
- Device Name
- Database Sync Date
- 2026-08-09 09:24:54
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of M915, Medikro Pro?
The registered manufacturer of record for M915, Medikro Pro is Medikro Oy.
What is the Primary UDI-DI identifier for M915, Medikro Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M9488.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Similar Classification Devices (BZG)
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