eudamed_udi Primary ID: 05407009800467

Multifonction Belt (UDI 05407009800467)

Manufactured by RENOL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Multifonction Belt (Model/Catalog Number: RFM23000) is a medical device manufactured by RENOL. This product is indexed under FDA Product Code / Category Classification V0804 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RFM23000
Product Code / EMDN: V0804
Device Name: Restraining system
Database Sync Date: 2026-08-09 17:07:46

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Multifonction Belt?

The registered manufacturer of record for Multifonction Belt is RENOL.

What is the Primary UDI-DI identifier for Multifonction Belt?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05407009800467.

What classification code is assigned to this device?

This device is registered under product classification code V0804.

Similar Classification Devices (V0804)

Other Devices by RENOL

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint