eudamed_udi
Primary ID: 06420099000486
Medikro Pressure Tube (UDI 06420099000486)
Manufactured by Medikro Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medikro Pressure Tube - Primary ID 06420099000486
Device Regulatory Overview
The Medikro Pressure Tube (Model/Catalog Number: M9264-200) is a medical device manufactured by Medikro Oy. This product is indexed under FDA Product Code / Category Classification Z12150185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M9264-200
- Product Code / EMDN
- Z12150185
- Device Name
- M9264
- Database Sync Date
- 2026-08-09 16:47:56
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 Pressure Tube?
The registered manufacturer of record for Medikro Pressure Tube is Medikro Oy.
What is the Primary UDI-DI identifier for Medikro Pressure Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06420099000486.
What classification code is assigned to this device?
This device is registered under product classification code Z12150185.
Similar Classification Devices (Z12150185)
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