eudamed_udi Primary ID: 05714879003066

HA MOJO MRR2D M7 TCBLK (UDI 05714879003066)

Manufactured by WSAUD A/S

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HA MOJO MRR2D M7 TCBLK (Model/Catalog Number: 21007507) is a medical device manufactured by WSAUD A/S. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 21007507
Product Code / EMDN: Y2145060102
Device Name: RIC
Database Sync Date: 2026-08-09 16:28:44

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 HA MOJO MRR2D M7 TCBLK?

The registered manufacturer of record for HA MOJO MRR2D M7 TCBLK is WSAUD A/S.

What is the Primary UDI-DI identifier for HA MOJO MRR2D M7 TCBLK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714879003066.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060102.

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