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Organization name
UDI-DI code
Reference / catalog number

Monobloc stretcher FERIA — Class I MDR by ROYAX, s.r.o.

MD Atlas
ROYAX, s.r.o.

EUDAMED last updated this device on Mar 17, 2026

Monobloc stretcher FERIA

859420820AMSTK8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ROYAX, s.r.o.
UDI-DI code: 08594208200208
Reference / catalog number: R-S-RS-FE-01

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Manufacturer information

Organization name: ROYAX, s.r.o.
SRN: CZ-MF-000020709
Manufacturer status: Active

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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.

Market distribution

Primary placement in Czechia; available across 1 country total.

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

Device identification

Trade name: Monobloc stretcher FERIA
UDI-DI code: 08594208200208
Basic UDI-DI: 859420820AMSTK8
Reference / catalog number: R-S-RS-FE-01
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: FERIA stretchers is device for patient handling during medical interventions, designed for transporting patients in a ground ambulance. The stretchers are used to transport patients to the ambulance and from the ambulance to the hospital or medical facility.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050103EMERGENCY AND TRAUMATOLOGY STRETCHERS

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

UDI-PI traceability

Batch number
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Manufacturing date
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