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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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Clinical Rules — 1 UDI-DI variant, MDD (Digitalis Mx BV)

MD Atlas
Digitalis Mx BV

Data from EUDAMED, last updated May 30, 2026

Clinical Rules

B-10023674ClinicalRulesRY

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: Digitalis Mx BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-10023674ClinicalRulesRY
Device name: Clinical Rules
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: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Digitalis Mx BV
SRN: NL-MF-000048580
Country: Netherlands
Email: digitalis@digitalis.nl
Phone: +31 20 575 46 60

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSJ4977BFT3DBTDFB18GSTKY

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

Clinical RulesD-10023674ClinicalRulesRY