eudamed_udi Primary ID: 04251992197261

Sitzhose T-Modell (UDI 04251992197261)

Manufactured by John GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Sitzhose T-Modell (Model/Catalog Number: GURT-07050-M-10-3) is a medical device manufactured by John GmbH. This product is indexed under FDA Product Code / Category Classification Y122406 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: GURT-07050-M-10-3
Product Code / EMDN: Y122406
Device Name: Gurtsysteme
Database Sync Date: 2026-08-09 16:48:33

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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Frequently Asked Questions

Who is the primary manufacturer of Sitzhose T-Modell?

The registered manufacturer of record for Sitzhose T-Modell is John GmbH.

What is the Primary UDI-DI identifier for Sitzhose T-Modell?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251992197261.

What classification code is assigned to this device?

This device is registered under product classification code Y122406.

Similar Classification Devices (Y122406)

Other Devices by John GmbH

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