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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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Ringpessar — 18 UDI-DI variants, MDR (Büttner-Frank GmbH)

MD Atlas
Büttner-Frank GmbH

Data from EUDAMED, last updated May 23, 2026

Ringpessar

425023490000106700QH

18 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: Büttner-Frank GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 425023490000106700QH
Device name: Ringpessar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 24, 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

18 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K0YD8SH2VK41PD3A1H5C5SWT

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

106901110464190222
106902110464191912
106903110464192575
106904110464193141
106905110464194831
106906110464195494
106907110464196060
106908110464197750
106909110464198316
106701110432845362
106702110432847618
106703110432848281
106704110432849971
106705110432850765
106706110432851331
106707110432853684
106708110432854250
106709111274740225