MIMOSA (UDI MIMOSA Pro)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MIMOSA (Model/Catalog Number: MIMOSA Pro) is a medical device manufactured by MIMOSA Diagnostics Inc. This product is indexed under FDA Product Code / Category Classification MUD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MIMOSA Pro
Product Code / EMDN: MUD
Device Name
Database Sync Date: 2026-08-09 09:50:05

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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Frequently Asked Questions

Who is the primary manufacturer of MIMOSA?

The registered manufacturer of record for MIMOSA is MIMOSA Diagnostics Inc.

What is the Primary UDI-DI identifier for MIMOSA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MIMOSA Pro.

What classification code is assigned to this device?

This device is registered under product classification code MUD.

Similar Classification Devices (MUD)

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