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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

Not applicable — IVDD — General IVDD by Mylab Oy

MD Atlas
Mylab Oy

EUDAMED last updated this device on Jun 27, 2025

Not applicable

B-06429830135906

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Mylab Oy
UDI-DI code: 06429830135906
Reference / catalog number: Not applicable

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Manufacturer information

Organization name: Mylab Oy
SRN: FI-MF-000048232
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: 06429830135906
Basic UDI-DI: B-06429830135906
Reference / catalog number: Not applicable
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: My+ verikeskus - Main system is LIS (laboratory information system) - Part of the a software module is a medical device as software (software component) Medical device component's in the software are: - Blood compatibility check - Type&screen functionality Other components in the software are LIS (laboratory information system) functionalities.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02079092VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

Not applicableB-06429830135913On the market

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.