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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 — 10 UDI-DI variants, MDR (Büttner-Frank GmbH)

MD Atlas
Büttner-Frank GmbH

Data from EUDAMED, last updated May 23, 2026

Würfel-Pessar

PP71862WP70

10 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: PP71862WP70
Device name: Würfel-Pessar
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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K0SB94FVSMETE622RSJFPJ43

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

106920110346163555
106921110346164121
106922110346165811
106923110346166474
106924110346167040
106925110346168730
106926110686971092
106927110686972782
106928110686970429
106929110686969635