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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

MGU-00003 — IVDR Class A IVDR by Grundium Oy

MD Atlas
Grundium Oy

EUDAMED last updated this device on Feb 21, 2025

MGU-00003

6429810590MGU00003MW

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Grundium Oy
UDI-DI code: 06429810590022
Reference / catalog number: MGU-00003

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Manufacturer information

Organization name: Grundium Oy
SRN: FI-MF-000005144
Manufacturer status: Active

Market distribution

Primary placement in Finland; available across 1 country total.

Country	On market since	Until
FinlandPrimary placement	Jun 12, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 06429810590022
Basic UDI-DI: 6429810590MGU00003MW
Reference / catalog number: MGU-00003
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0202050304DIGITAL LABORATORY MICROSCOPES

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

MGU-000056429810590MGU00005N2On the market MGU-300096429810590MGU30009PBOn the market MGU-300086429810590MGU30008P9On 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.