eudamed_udi Primary ID: 05407009800450

Lateral Long Extender Belt (UDI 05407009800450)

Manufactured by RENOL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lateral Long Extender Belt (Model/Catalog Number: RFE24500RL) 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: RFE24500RL
Product Code / EMDN: V0804
Device Name: Restraining system
Database Sync Date: 2026-08-09 17:31:52

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 Lateral Long Extender Belt?

The registered manufacturer of record for Lateral Long Extender Belt is RENOL.

What is the Primary UDI-DI identifier for Lateral Long Extender Belt?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05407009800450.

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

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