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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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JOSI-Wismi / JOSI-Stroller Reha-Karre — 3 UDI-DI variants, MDR

MD Atlas
John GmbH

Data from EUDAMED, last updated May 23, 2026

JOSI-Wismi / JOSI-Stroller Reha-Karre

42519921ReKaWI2T

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: John GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42519921ReKaWI2T
Device name: JOSI-Wismi / JOSI-Stroller Reha-Karre
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: John GmbH
SRN: DE-MF-000012375
Country: Germany
Email: hugo.dewit@johngmbh.com
Phone: +49 36923 8388-0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K772WJ1WPEYBB1Q569EZQ6PX

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

JW-1000204251992100025
JW-1000104251992100018
JW-1000304251992100032