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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

AINO Ennakoivan hoidon… — Class I MDR by Mehiläinen Oy

MD Atlas
Mehiläinen Oy

EUDAMED last updated this device on Dec 11, 2024

AINO Ennakoivan hoidon toimintamalli

642981120300AINO00UQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Mehiläinen Oy
UDI-DI code: 06429811203013
Reference / catalog number: AINO Ennakoivan hoidon toimintamalli

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Manufacturer information

Organization name: Mehiläinen Oy
SRN: FI-MF-000037905
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: 06429811203013
Basic UDI-DI: 642981120300AINO00UQ
Reference / catalog number: AINO Ennakoivan hoidon toimintamalli
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Aino is intended to be used to identify an individual potentially in need of healthcare services based on the information in the data storage, and it is suitable to be used on all individuals with available information
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.