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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

VPPRODID552WAR9547 — Class I MDR by VEST-POL Group Sp. z…

MD Atlas
VEST-POL Group Sp. z o.o.

EUDAMED last updated this device on Apr 14, 2026

VPPRODID552WAR9547

590515557PLASZCZKAZ7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VEST-POL Group Sp. z o.o.
UDI-DI code: 05905155579027
Reference / catalog number: VPPRODID552WAR9547

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View device family (Basic UDI)

Manufacturer information

Organization name: VEST-POL Group Sp. z o.o.
SRN: PL-MF-000003439
Manufacturer status: Active

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VPPRODID109WAR3804590515557KOLDRAJPOn the market VPPRODID56590515557DUSZEKNAOn the market VPPRODID57590515557DUSZEKNAOn the market VPPRODID58590515557DUSZEKNAOn the market VPPRODID59590515557DUSZEKNAOn the market

Critical warnings

No critical warnings reported for this device.

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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: not provided
UDI-DI code: 05905155579027
Basic UDI-DI: 590515557PLASZCZKAZ7
Reference / catalog number: VPPRODID552WAR9547
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: Koc obciążeniowy Płaszczka "Manty", szerokość: ok.115 cm, długość: ok. 120 cm, wypełnienie: żwirek naturalny, tkanina: minky z wypustkami (warstwa zewnętrzna), minky gładka (warstwa wewnętrzna), kolorystyka - do wyboru
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 120 MU10
115 MU10

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.

Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER

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

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.