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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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Duocare — 4 UDI-DI variants, MDR

MD Atlas
JMS- Indústria de Mobiliário Hospitalar, SA

Data from EUDAMED, last updated May 31, 2026

Duocare

560039857DUOCAREPK

4 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: JMS- Indústria de Mobiliário Hospitalar, SA

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 560039857DUOCAREPK
Device name: Duocare
Device model: Duocare
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: JMS- Indústria de Mobiliário Hospitalar, SA
SRN: PT-MF-000006022
Country: Portugal
Email: smortagua@jmsadicocare.com
Phone: +351234880018

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRP71RNJ9MEZM7X5PM7CGVMX

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

Duocare Hospital Bed05600398572216
Duocare Hospital Bed05600398572186
Duocare Hospital Bed05600398572209
Duocare Hospital Bed05600398572193