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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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Zange, dental / Forceps dental — 107 UDI-DI variants, MDR

MD Atlas
REDA Instrumente GmbH

Data from EUDAMED, last updated May 31, 2026

Zange, dental / Forceps dental

4063058000001173R

107 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: 4063058000001173R
Device name: Zange, dental / Forceps dental
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

107 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSM177BHA8PJTVPJPWSZ3GME

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

87021-3904063058164106
87000-2204063058163512
87020-51S04063058164083
87100-1604063058164151
87000-35N04063058163604
87102-2204063058164403
87101-51AS04063058164373

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