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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

Smart Symptom Check — Class IIa MDR by JST Healthcare…

MD Atlas
JST Healthcare Solutions Oy

EUDAMED last updated this device on Jan 29, 2026

Smart Symptom Check

64298301792JSTSSYMPTOMCFK

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: JST Healthcare Solutions Oy
UDI-DI code: 06429830179214
Reference / catalog number: Smart Symptom Check

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Manufacturer information

Organization name: JST Healthcare Solutions Oy
SRN: FI-MF-000011817
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 2 countries total.

Country	On market since	Until
FinlandPrimary placement	Jan 29, 2026	Still on market
Sweden	Jan 29, 2026	Still on market

Device identification

Trade name: Smart Symptom Check
UDI-DI code: 06429830179214
Basic UDI-DI: 64298301792JSTSSYMPTOMCFK
Reference / catalog number: Smart Symptom Check
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Smart Symptom Check software drives the assessment of the need for treatment. Smart symptom check provides information to healthcare professionals and patients by generating a summary report on patient’s answers, of patient’s possible conditions, the clinical urgency and care path options appropriate to the situation.
Additional information URL: https://s3.eu-north-1.amazonaws.com/com.smartsymtomcheck.manuals/index.html
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.