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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

Refrigerated and heated… — IVDR Class A IVDR

MD Atlas
"MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY

EUDAMED last updated this device on Apr 6, 2023

Refrigerated and heated laboratory centrifuge MPW-260RH 110V/60Hz

590538636-IVD-CEN-007-6F

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY
UDI-DI code: 05905386360364
Reference / catalog number: 10260RH/1-6/110

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View device family (Basic UDI)

Manufacturer information

Organization name: "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY
SRN: PL-MF-000032831
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 1 country total.

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

Device identification

Trade name: Refrigerated and heated laboratory centrifuge MPW-260RH 110V/60Hz
UDI-DI code: 05905386360364
Basic UDI-DI: 590538636-IVD-CEN-007-6F
Reference / catalog number: 10260RH/1-6/110
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: https://www.mpw.pl/
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.

W02069005REFRIGERATED CENTRIFUGES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.