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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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Würfel-Pessar, Sieb — 9 UDI-DI variants, MDR (Büttner-Frank GmbH)

MD Atlas
Büttner-Frank GmbH

Data from EUDAMED, last updated May 23, 2026

Würfel-Pessar, Sieb

PP71862WPS13

9 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Büttner-Frank GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP71862WPS13
Device name: Würfel-Pessar, Sieb
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Büttner-Frank GmbH
SRN: DE-MF-000006203
Country: Germany
Email: info@buettner-frank.de
Phone: +49 9131 79050

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K0S88K5T89QXM1NXFT1BZ4VW

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

106820110492560564
106822110492562820
106823110492563483
106824110492564049
106825110492565739
106826110686973348
106827110686975604
106828110686976267
106829110686977957