gudid
Primary ID: 191004
ergoselect 5 (UDI 191004)
Manufactured by ergoline GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ergoselect 5 - Primary ID 191004
Device Regulatory Overview
The ergoselect 5 (Model/Catalog Number: 191004) 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
- 191004
- Product Code / EMDN
- ISD
- Device Name
- Database Sync Date
- 2026-08-09 09:11:48
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 ergoselect 5?
The registered manufacturer of record for ergoselect 5 is ergoline GmbH.
What is the Primary UDI-DI identifier for ergoselect 5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 191004.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint