eudamed_udi Primary ID: 05714880151206

HA MAGNIFY MBB2 M04 SRED (UDI 05714880151206)

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 MAGNIFY MBB2 M04 SRED (Model/Catalog Number: 21010428) is a medical device manufactured by WSAUD A/S. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 21010428
Product Code / EMDN: Y2145060101
Device Name: BTE
Database Sync Date: 2026-08-09 16:28:47

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 MAGNIFY MBB2 M04 SRED?

The registered manufacturer of record for HA MAGNIFY MBB2 M04 SRED is WSAUD A/S.

What is the Primary UDI-DI identifier for HA MAGNIFY MBB2 M04 SRED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880151206.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060101.

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