gudid
Primary ID: 2017911-301
ERGOMETER EBIKE III Basic (UDI 2017911-301)
Manufactured by ergoline GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERGOMETER EBIKE III Basic - Primary ID 2017911-301
Device Regulatory Overview
The ERGOMETER EBIKE III Basic (Model/Catalog Number: 2017911-301) 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
- 2017911-301
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ERGOMETER EBIKE III Basic?
The registered manufacturer of record for ERGOMETER EBIKE III Basic is ergoline GmbH.
What is the Primary UDI-DI identifier for ERGOMETER EBIKE III Basic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2017911-301.
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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