Lode B.V. (UDI 967941)

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: 967941) 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: 967941
Product Code / EMDN: ISD
Device Name: 967941 Angio imaging - with stress support ultrasound (110V)
Database Sync Date: 2026-08-09 09:26:51

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 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 967941.

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.

Programmatic Export

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

JSON API Endpoint