Resonance (UDI RE-VO2)

Manufactured by M.R.S. SRL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Resonance (Model/Catalog Number: RE-VO2) is a medical device manufactured by M.R.S. SRL. This product is indexed under FDA Product Code / Category Classification ERA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RE-VO2
Product Code / EMDN: ERA
Device Name: USB VIDEO OTOSCOPE
Database Sync Date: 2026-08-09 09:04:32

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 Resonance?

The registered manufacturer of record for Resonance is M.R.S. SRL.

What is the Primary UDI-DI identifier for Resonance?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RE-VO2.

What classification code is assigned to this device?

This device is registered under product classification code ERA.

Similar Classification Devices (ERA)

Other Devices by M.R.S. SRL

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