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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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Resectoscope tubes — 6 UDI-DI variants, MDR (Richard Wolf GmbH)

MD Atlas
Richard Wolf GmbH

Data from EUDAMED, last updated May 23, 2026

Resectoscope tubes

405520727052019-0018183PD

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: Richard Wolf GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 405520727052019-0018183PD
Device name: Resectoscope tubes
Device model: 10000201233
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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K9HX920C95K1Y2D1PN6VWJSC

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

8834.03504055207043295
8834.07504055207043356
8834.05504055207043318
8834.01504055207043257
8834.02504055207043271
8834.08504055207043370