gudid
Primary ID: FR1MZ1-B
Microlife (UDI FR1MZ1-B)
Manufactured by MICROLIFE USA, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Microlife - Primary ID FR1MZ1-B
Device Regulatory Overview
The Microlife (Model/Catalog Number: FR1MZ1-B) is a medical device manufactured by MICROLIFE USA, INC.. This product is indexed under FDA Product Code / Category Classification SDV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FR1MZ1-B
- Product Code / EMDN
- SDV
- Device Name
- Database Sync Date
- 2026-08-09 09:15:29
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 USA, INC..
What is the Primary UDI-DI identifier for Microlife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FR1MZ1-B.
What classification code is assigned to this device?
This device is registered under product classification code SDV.
Similar Classification Devices (SDV)
Other Devices by MICROLIFE USA, INC.
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