eudamed_udi Primary ID: 06432100002495

Remo-Wax (UDI 06432100002495)

Manufactured by Orion Oyj

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Remo-Wax (Model/Catalog Number: 112116) is a medical device manufactured by Orion Oyj. This product is indexed under FDA Product Code / Category Classification Q030499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 112116
Product Code / EMDN: Q030499
Device Name: Remo-Wax
Database Sync Date: 2026-08-09 18:30:19

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 Remo-Wax?

The registered manufacturer of record for Remo-Wax is Orion Oyj.

What is the Primary UDI-DI identifier for Remo-Wax?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06432100002495.

What classification code is assigned to this device?

This device is registered under product classification code Q030499.

Similar Classification Devices (Q030499)

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