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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

LUFFY 2 — Class I MDR by TORUSCARE Sp. z o.o.

MD Atlas
TORUSCARE Sp. z o.o.

EUDAMED last updated this device on Aug 22, 2025

LUFFY 2

590218602MEDCHAIRP5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TORUSCARE Sp. z o.o.
UDI-DI code: 05902186020863
Reference / catalog number: WC1036587

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Manufacturer information

Organization name: TORUSCARE Sp. z o.o.
SRN: PL-MF-000047801
Manufacturer status: Active

Related devices

ACCOIN 1590218602MEDCHAIRP5On the market ACCOIN 2590218602MEDCHAIRP5On the market ACCOIN 3590218602MEDCHAIRP5On the market ACCOIN 4590218602MEDCHAIRP5On the market ACCOIN 5590218602MEDCHAIRP5On 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.

Critical warnings

No critical warnings reported for this device.

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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: LUFFY 2
UDI-DI code: 05902186020863
Basic UDI-DI: 590218602MEDCHAIRP5
Reference / catalog number: WC1036587
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on 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.

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.

Y122103PUSH WHEELCHAIRS

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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