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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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DISCHER Master — 8 UDI-DI variants, MDR (DISCHER Technik GmbH)

MD Atlas
DISCHER Technik GmbH

Data from EUDAMED, last updated May 23, 2026

DISCHER Master

426073425-RDA-TV

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: DISCHER Technik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426073425-RDA-TV
Device name: DISCHER Master
Device model: Master
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: DISCHER Technik GmbH
SRN: DE-MF-000004972
Country: Germany
Email: olaf.discher@discher.de
Phone: +49 2104 2336-0

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KJ4SM6KXJN63AJ95CMVNE18C

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

20212 / 20213 04260734250034
20218 / 2021904260734250058
20214 / 20215 / 20216 / 2021704260734250041
2022004260734250089
20204 / 20205 / 20206 / 2020704260734250010
20208 / 20209 / 20210 / 2021104260734250027
20222 / 2022304260734250065
20224 / 20225 / 20226 / 2022704260734250072