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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

Functional trolley — Class I MDR by Tribo sp. z o.o.

MD Atlas
Tribo sp. z o.o.

EUDAMED last updated this device on Dec 5, 2024

Functional trolley

5905141346WKFL

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Tribo sp. z o.o.
UDI-DI code: 05905141346213
Reference / catalog number: WK7000

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View device family (Basic UDI)

Manufacturer information

Organization name: Tribo sp. z o.o.
SRN: PL-MF-000026942
Manufacturer status: Active

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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: Functional trolley
UDI-DI code: 05905141346213
Basic UDI-DI: 5905141346WKFL
Reference / catalog number: WK7000
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: A cart that contains a variety of equipment, anaesthetic agents, and other supplies that are readily available to the anaesthetist in order to meet the diverse needs of patients in scheduled procedures as well as in emergencies. The trolley (cart) has a work surface that can be easily cleaned and that provides an area to display equipment (e.g., laryngoscope and blades, endotracheal (ET) tubes, stethoscopes). This wheeled cart has drawers, shelves, and compartments with doors that are organized to hold individual drugs, devices, and instruments.
Additional information URL: https://www.tribo.com.pl/
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)05905141346213

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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.

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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.