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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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Organization name
UDI-DI code
Reference / catalog number

Remecare — Class IIa MDD by REMECARE BV

MD Atlas
REMECARE BV

EUDAMED last updated this device on Feb 3, 2026

Remecare

B-05419980240507

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: REMECARE BV
UDI-DI code: 05419980240507
Reference / catalog number: Remecare

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Manufacturer information

Organization name: REMECARE BV
SRN: BE-MF-000018364
Manufacturer status: Active

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	May 4, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05419980240507
Basic UDI-DI: B-05419980240507
Reference / catalog number: Remecare
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Remecare is intended for telemonitoring vital and non-vital parameters of home-based patients
Additional information URL: https://www.remecare.be/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.