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Organization name
UDI-DI code
Reference / catalog number

Magnetronic MF-2 — Class IIa MDR by Elektronika i…

MD Atlas
Elektronika i Elektromedycyna M.Lewandowski Sp.J.

EUDAMED last updated this device on Apr 8, 2026

Magnetronic MF-2

5906660092MF2B8

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Elektronika i Elektromedycyna M.Lewandowski Sp.J.
UDI-DI code: 05906660092346
Reference / catalog number: Magnetronic MF-2

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View device family (Basic UDI)

Manufacturer information

Organization name: Elektronika i Elektromedycyna M.Lewandowski Sp.J.
SRN: PL-MF-000032400
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.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: Magnetronic MF-2
UDI-DI code: 05906660092346
Basic UDI-DI: 5906660092MF2B8
Reference / catalog number: Magnetronic MF-2
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: MAGNETRONIC MF–2 is a modern, microprocessor controlled unit for magnetotherapy. It can work with various types of magnetic field applicators.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05906660092346

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

Z120606MAGNETOTHERAPY EQUIPMENT

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

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Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0030/2034/2025Issued
Quality management systemNotified body: 2274Expiry: Jan 16, 2028