GUDIDData
eudamed_udi Primary ID: 04251816802210

HK-2065/3Y (UDI 04251816802210)

Manufactured by AGA Sanitätsartikel GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HK-2065/3Y - Primary ID 04251816802210

Device Regulatory Overview

The HK-2065/3Y (Model/Catalog Number: 87) 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
87
Product Code / EMDN
V080699
Device Name
Liege
Database Sync Date
2026-08-09 16:30:42

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 HK-2065/3Y?

The registered manufacturer of record for HK-2065/3Y is AGA Sanitätsartikel GmbH.

What is the Primary UDI-DI identifier for HK-2065/3Y?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816802210.

What classification code is assigned to this device?

This device is registered under product classification code V080699.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint