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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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Filtration Stand Electric — 2 UDI-DI variants, MDR (STRUB GMBH)

MD Atlas
STRUB GMBH

Data from EUDAMED, last updated May 23, 2026

Filtration Stand Electric

42519192-EQP-FST-ELEAY

2 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: STRUB GMBH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42519192-EQP-FST-ELEAY
Device name: Filtration Stand Electric
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: STRUB GMBH
SRN: DE-MF-000034376
Country: Germany
Email: contact@strub-group.com
Phone: +49 6349928637

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JPVW0Q658TEKNHH5Q9A85ZEA

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

SLEN-0001-STD-K0204251919200302
SLEN-0001-STD-K0104251919200401