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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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Epi-Care — 3 UDI-DI variants, MDR (Danish Care Technology ApS)

MD Atlas
Danish Care Technology ApS

Data from EUDAMED, last updated May 23, 2026

Epi-Care

57000023047EpiCareQ2

3 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: Danish Care Technology ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 57000023047EpiCareQ2
Device name: Epi-Care
Device model: Epi-Care free 4G
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: Danish Care Technology ApS
SRN: DK-MF-000049214
Country: Denmark
Email: info@danishcare.dk

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KHNJZ2G4HCJEBWVPARXCM8NE

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

101008205700002304735
101008405700002304728
101007005700002304742