Lode B.V. (UDI 969901)

Manufactured by Lode B.V.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lode B.V. (Model/Catalog Number: 969901) is a medical device manufactured by Lode B.V.. This product is indexed under FDA Product Code / Category Classification ISD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 969901
Product Code / EMDN: ISD
Device Name: 969901 Corival Recumbent rehab
Database Sync Date: 2026-08-09 09:26:51

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 Lode B.V.?

The registered manufacturer of record for Lode B.V. is Lode B.V..

What is the Primary UDI-DI identifier for Lode B.V.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 969901.

What classification code is assigned to this device?

This device is registered under product classification code ISD.

Similar Classification Devices (ISD)

Other Devices by Lode B.V.

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