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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

60702 — Class I MDD by StellarQ Ltd

MD Atlas
StellarQ Ltd

EUDAMED last updated this device on Dec 20, 2021

60702

B-06429830118800

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: StellarQ Ltd
UDI-DI code: 06429830118800
Reference / catalog number: 60702

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Manufacturer information

Organization name: StellarQ Ltd
SRN: FI-MF-000011208
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Placed on the market in Finland; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 06429830118800
Basic UDI-DI: B-06429830118800
Reference / catalog number: 60702
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: StellarQ is a software for managing chronic diseases and rehabilitations. It is delivered to healthcare units as a Software as a Service (SaaS). The service supports healthcare professionals in making the right diagnosis, indicates potential changes in disease progression and enables monitoring the clinical course of a disease and evaluating the effectiveness of treatment and rehabilitation. The service is integrated with the core systems of healthcare organisations. The service has two interfaces, one for healthcare professionals and one for patients (PROM/PREM).
Additional information URL: No additional information URL provided by the manufacturer.
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.