gudid
Primary ID: 161801
ers2 Basic Software (UDI 161801)
Manufactured by ergoline GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ers2 Basic Software - Primary ID 161801
Device Regulatory Overview
The ers2 Basic Software (Model/Catalog Number: 161801) is a medical device manufactured by ergoline GmbH. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 161801
- Product Code / EMDN
- DRG
- 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 ers2 Basic Software?
The registered manufacturer of record for ers2 Basic Software is ergoline GmbH.
What is the Primary UDI-DI identifier for ers2 Basic Software?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 161801.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by ergoline GmbH
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