eudamed_udi Primary ID: 04251992100001

Unspecified Brand (UDI 04251992100001)

Manufactured by John GmbH

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 02000-05000-00300) is a medical device manufactured by John GmbH. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 02000-05000-00300
Product Code / EMDN: Y061209
Device Name: Kniekissen mit Befestigungsband
Database Sync Date: 2026-08-09 17:40:26

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is John GmbH.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251992100001.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Similar Classification Devices (Y061209)

Other Devices by John GmbH

Programmatic Export

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

JSON API Endpoint