eudamed_udi Primary ID: 05407009800894

Limb Hoders (UDI 05407009800894)

Manufactured by RENOL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Limb Hoders (Model/Catalog Number: RFL15000RL) 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: RFL15000RL
Product Code / EMDN: V0804
Device Name: Restraining system
Database Sync Date: 2026-08-09 17:19:35

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 Limb Hoders?

The registered manufacturer of record for Limb Hoders is RENOL.

What is the Primary UDI-DI identifier for Limb Hoders?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05407009800894.

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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