eudamed_udi Primary ID: 05714880292190

HA ALLURE ARRD2 330 TMGR (UDI 05714880292190)

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 ALLURE ARRD2 330 TMGR (Model/Catalog Number: 21048844) 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: 21048844
Product Code / EMDN: Y2145060102
Device Name: RIC
Database Sync Date: 2026-08-09 16:28:50

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 ALLURE ARRD2 330 TMGR?

The registered manufacturer of record for HA ALLURE ARRD2 330 TMGR is WSAUD A/S.

What is the Primary UDI-DI identifier for HA ALLURE ARRD2 330 TMGR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880292190.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060102.

Similar Classification Devices (Y2145060102)

Other Devices by WSAUD A/S

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