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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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Raspel, Nase / Rasp, Nose — 40 UDI-DI variants, MDR

MD Atlas
REDA Instrumente GmbH

Data from EUDAMED, last updated May 31, 2026

Raspel, Nase / Rasp, Nose

4063058000000894D

40 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: 4063058000000894D
Device name: Raspel, Nase / Rasp, Nose
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 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

40 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJGB88Y9WK7NWENXE1BNAFZ

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

47524-0104063058086279
47521-0304063058044736
47526-2004063058086576
47505-1804063058086668
47522-0104063058044743
47523-0104063058077529
47504-1804063058044613
47526-1604063058044774
47525-2004063058084336
47523-0204063058077536
47506-1804063058086675
47522-0904063058044767
47521-0204063058044729
47527-1604063058044781
47514-1604063058044675

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