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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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MijnVital10 — 1 UDI-DI variant, MDD (Simal Beheer B.V.)

MD Atlas
Simal Beheer B.V.

Data from EUDAMED, last updated May 30, 2026

MijnVital10

B-NL-MF-0000423337T

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Simal Beheer B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: B-NL-MF-0000423337T
Device name: MijnVital10
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Special device type: refdata.special-mdd-device-type.software
Version date: Jun 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Simal Beheer B.V.
SRN: NL-MF-000042333
Country: Netherlands
Email: michael.eichelsheim@zotikos.nl

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J1CQGYMQ64RS22D7QBANETC1

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

MijnVital10D-NL-MF-0000423337T