eudamed_udi
Primary ID: 04251816801961
H-EKA 1080/Y 900 (UDI 04251816801961)
Manufactured by AGA Sanitätsartikel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for H-EKA 1080/Y 900 - Primary ID 04251816801961
Device Regulatory Overview
The H-EKA 1080/Y 900 (Model/Catalog Number: 65) is a medical device manufactured by AGA Sanitätsartikel GmbH. This product is indexed under FDA Product Code / Category Classification V080699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 65
- Product Code / EMDN
- V080699
- Device Name
- Liege
- Database Sync Date
- 2026-08-09 16:45:40
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 H-EKA 1080/Y 900?
The registered manufacturer of record for H-EKA 1080/Y 900 is AGA Sanitätsartikel GmbH.
What is the Primary UDI-DI identifier for H-EKA 1080/Y 900?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816801961.
What classification code is assigned to this device?
This device is registered under product classification code V080699.
Similar Classification Devices (V080699)
Other Devices by AGA Sanitätsartikel GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint