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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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Kürette / Curette — 481 UDI-DI variants, MDR (REDA Instrumente GmbH)

MD Atlas
REDA Instrumente GmbH

Data from EUDAMED, last updated May 31, 2026

Kürette / Curette

4063058000000243H

481 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: REDA Instrumente GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 4063058000000243H
Device name: Kürette / Curette
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: REDA Instrumente GmbH
SRN: DE-MF-000005592
Country: Germany
Email: thomas.benas@reda-instrumente.de

Variants by status

UDI-DI variants

481 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSM201WRF6VVWXPTPMCR7D4J

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

33474-1304063058240473
47388-0404063058096551
33483-0104063058023731
33480-9704063058023588
RD-126804063058222622
33479-0604063058023571