eudamed_udi Primary ID: 04251992100032

JOSI-Wismi (UDI 04251992100032)

Manufactured by John GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The JOSI-Wismi (Model/Catalog Number: JW-10003) is a medical device manufactured by John GmbH. This product is indexed under FDA Product Code / Category Classification Y122103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: JW-10003
Product Code / EMDN: Y122103
Device Name: JOSI-Wismi / JOSI-Stroller Reha-Karre
Database Sync Date: 2026-08-09 16:58:34

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 JOSI-Wismi?

The registered manufacturer of record for JOSI-Wismi is John GmbH.

What is the Primary UDI-DI identifier for JOSI-Wismi?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251992100032.

What classification code is assigned to this device?

This device is registered under product classification code Y122103.

Similar Classification Devices (Y122103)

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