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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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IPOMAX — 16 UDI-DI variants, MDR (WWS Ideen aus PU GmbH)

MD Atlas
WWS Ideen aus PU GmbH

Data from EUDAMED, last updated May 23, 2026

IPOMAX

4262487769105BVW

16 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: WWS Ideen aus PU GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4262487769105BVW
Device name: IPOMAX
Device model: 9105207
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: WWS Ideen aus PU GmbH
SRN: DE-MF-000043534
Country: Germany
Email: info@wws-windeisen.de
Phone: +49 7141 29 866 90

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JNH8GD4EM098S6T1EG24VEGC

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

910520204262487760044
910520404262487760068
910501704262487760105
910520804262487760020
910521404262487760112
910521204262487760143
910521104262487760136
910501804262487760099
910520604262487760082
910520104262487760037
910520504262487760075
910521004262487760150
910520704262487760167
910520904262487760013
910521304262487760129
910520304262487760051