eudamed_udi
Primary ID: 04719003932589
Microlife (UDI 04719003932589)
Manufactured by Microlife Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Microlife - Primary ID 04719003932589
Device Regulatory Overview
The Microlife (Model/Catalog Number: CA3-W0-C44) is a medical device manufactured by Microlife Corporation. This product is indexed under FDA Product Code / Category Classification Z1203020599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CA3-W0-C44
- Product Code / EMDN
- Z1203020599
- Device Name
- Cuff for Digital Non-invasive Blood Pressure Monitor
- Database Sync Date
- 2026-08-09 16:58:27
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 Microlife?
The registered manufacturer of record for Microlife is Microlife Corporation.
What is the Primary UDI-DI identifier for Microlife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719003932589.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020599.
Similar Classification Devices (Z1203020599)
Other Devices by Microlife Corporation
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