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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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Pinzetten / Tweezers — 710 UDI-DI variants, MDR

MD Atlas
REDA Instrumente GmbH

Data from EUDAMED, last updated May 31, 2026

Pinzetten / Tweezers

40630580000014742

710 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: 40630580000014742
Device name: Pinzetten / Tweezers
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

710 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSM28TYT9PV5TP3DV0R2QBPQ

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

RD-1677T04063058227290
91160-10N04063058087467
RD-179804063058229034
18153-0104063058210919
43841-1004063058038971
12090-21D04063058085708
11187-2004063058007120
93304-2404063058067995
44068-0904063058039442
11104-2504063058006376