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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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Zubehör — 6 UDI-DI variants, MDR (Wieds Ecochem AG)

MD Atlas
Wieds Ecochem AG

Data from EUDAMED, last updated May 23, 2026

Zubehör

PP11961ZUBEHOER50

6 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: Wieds Ecochem AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP11961ZUBEHOER50
Device name: Zubehör
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Wieds Ecochem AG
SRN: DE-MF-000006539
Country: Germany
Email: labor@wieds.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01H0FQ717DAHRVY9AFJ6Z6GJRS

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

M 70189611311961M7018961W55043
M 7018963PP11961M701896392
M 6009530 TID1311961M6009530TID026
M 70193701311961M7019370073
M 70193691311961M7019369008
M 70193711311961M7019371089