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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

230.3.000/IVD (230V) — IVDR Class A IVDR by DOMEL, d.o.o.

MD Atlas
DOMEL, d.o.o.

EUDAMED last updated this device on Mar 18, 2025

230.3.000/IVD (230V)

383008323CENTRIFUGEWD

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DOMEL, d.o.o.
UDI-DI code: 03830083230097
Reference / catalog number: 230.3.000/IVD (230V)

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View device family (Basic UDI)

Manufacturer information

Organization name: DOMEL, d.o.o.
SRN: SI-MF-000030074
Manufacturer status: Active

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW008
Device may get contaminated by infectious materials.
CW010
Read the instructions before use.
CW257
Be careful when closing the lid of the centrifuge.

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Market distribution

Primary placement in Slovenia; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 03830083230097
Basic UDI-DI: 383008323CENTRIFUGEWD
Reference / catalog number: 230.3.000/IVD (230V)
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: Centrifuge CENTRIC MF 48 IVD is a laboratory centrifuge intended to be used at in vitro diagnostic examinations in laboratories for separating the substances with different specific densities by centrifugal force.
Additional information URL: https://www.domel.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W02069003CENTRIFUGES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Related devices

472.3.000/IVD (230V)383008323CENTRIFUGEWDOn the market 473.3.000/IVD (230V)383008323CENTRIFUGEWDOn the market 232.3.005/IVD (230V)383008323CENTRIFUGEWDOn the market 232.3.010/IVD (230V)383008323CENTRIFUGEWDOn the market 230.3.500/IVD (230V)383008323CENTRIFUGEWDOn 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.