eudamed_udi
Primary ID: 04251816800988
EKG-3080/3 (UDI 04251816800988)
Manufactured by AGA Sanitätsartikel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EKG-3080/3 - Primary ID 04251816800988
Device Regulatory Overview
The EKG-3080/3 (Model/Catalog Number: 49) is a medical device manufactured by AGA Sanitätsartikel GmbH. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 49
- Product Code / EMDN
- V080602
- Device Name
- Liege
- Database Sync Date
- 2026-08-09 16:49:14
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 EKG-3080/3?
The registered manufacturer of record for EKG-3080/3 is AGA Sanitätsartikel GmbH.
What is the Primary UDI-DI identifier for EKG-3080/3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816800988.
What classification code is assigned to this device?
This device is registered under product classification code V080602.
Similar Classification Devices (V080602)
Other Devices by AGA Sanitätsartikel GmbH
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