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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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ViMeDat Reflux- und Motilitätsanalyse-P… — 12 UDI-DI variants, MDR

MD Atlas
Standard Instruments GmbH

Data from EUDAMED, last updated May 23, 2026

ViMeDat Reflux- und Motilitätsanalyse-Plattform

426018106VRMPA8

12 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: Standard Instruments GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426018106VRMPA8
Device name: ViMeDat Reflux- und Motilitätsanalyse-Plattform
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Standard Instruments GmbH
SRN: DE-MF-000013833
Country: Germany
Email: regulatory@stdi.de

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KNKHPEWDPSERMV6W6KD0YM8B

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

SI-ZNIS-M04260181060088
SI-ZNIS-L04260181060095
SI-SNIS04260181060026
SI-SNID1004260181060057
SI-SNIS-S04260181060033
SI-SNID1504260181060064
SI-ZNID-L04260181060101
SI-ZNIS-S04260181060071
SI-SNID0504260181060040
ViMeDat04260181060002
ZALT04260181060019
VRMP04260181060187