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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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Adapters — 3 UDI-DI variants, MDR (Richard Wolf GmbH)

MD Atlas
Richard Wolf GmbH

Data from EUDAMED, last updated May 23, 2026

Adapters

405520727052019-0018179PN

3 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: Richard Wolf GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 405520727052019-0018179PN
Device name: Adapters
Device model: 10000201232
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Richard Wolf GmbH
SRN: DE-MF-000007048
Country: Germany
Email: info@richard-wolf.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K9HRWQWTNBYZMCCJ69MER6A2

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

8791.75104055207020678
8792.45204055207020715
8792.45104055207020708