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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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Instrumententisch — 35 UDI-DI variants, MDR

MD Atlas
Wagner & Guder Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Instrumententisch

426073094TABLE8E

35 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: Wagner & Guder Medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426073094TABLE8E
Device name: Instrumententisch
Device model: Instrumententisch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Wagner & Guder Medical GmbH
SRN: DE-MF-000009554
Country: Germany
Email: info@wagner-guder-medical.de
Phone: +493644515561

Variants by status

UDI-DI variants

35 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMMZMXRE8HW9NXK30NZT3BPT

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

ST-36504260760940336
ST-37004260760940343
ST-37104260760940350
ST-37204260760940367
ST-44004260760940398
ST-440_11504260760940473
ST-44504260760940404
ST-445_11504260760940480
ST-45004260760940305
ST-50004260760940428

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