Lode B.V. (UDI 967923)

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: 967923) 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: 967923
Product Code / EMDN: ISD
Device Name: 967903 Angio cpet electrical wall fixation
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 967923.

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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