gudid Primary ID: 2017911-204

ERGOMETER EBIKE BASIC US & BP (UDI 2017911-204)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ERGOMETER EBIKE BASIC US & BP (Model/Catalog Number: 2017911-204) is a medical device manufactured by ergoline GmbH. This product is indexed under FDA Product Code / Category Classification ISD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2017911-204
Product Code / EMDN: ISD
Device Name
Database Sync Date: 2026-08-09 09:11:48

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 ERGOMETER EBIKE BASIC US & BP?

The registered manufacturer of record for ERGOMETER EBIKE BASIC US & BP is ergoline GmbH.

What is the Primary UDI-DI identifier for ERGOMETER EBIKE BASIC US & BP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2017911-204.

What classification code is assigned to this device?

This device is registered under product classification code ISD.

Similar Classification Devices (ISD)

Other Devices by ergoline GmbH

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