gudid
Primary ID: 192001
ergoselect 12 (UDI 192001)
Manufactured by ergoline GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ergoselect 12 - Primary ID 192001
Device Regulatory Overview
The ergoselect 12 (Model/Catalog Number: 192001) 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
- 192001
- 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 ergoselect 12?
The registered manufacturer of record for ergoselect 12 is ergoline GmbH.
What is the Primary UDI-DI identifier for ergoselect 12?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 192001.
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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