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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

M302V101M02 — Class I MDR by MEDIROL s.r.o.

MD Atlas
MEDIROL s.r.o.

EUDAMED last updated this device on Mar 27, 2026

M302V101M02

859420773VIVERAM302XB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIROL s.r.o.
UDI-DI code: 08594207730935
Reference / catalog number: M302V101M02

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Manufacturer information

Organization name: MEDIROL s.r.o.
SRN: CZ-MF-000006450
Manufacturer status: Active

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M302V202M01859420773VIPER2M302NXOn the market M302V202M02859420773VIPER2M302NXOn the market M302V201M02859420773VIPER2M302NXOn the market M302V201M01859420773VIPER2M302NXOn the market P402V203M01859420773VIPER2P402PROn 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 08594207730935
Basic UDI-DI: 859420773VIVERAM302XB
Reference / catalog number: M302V101M02
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: The VIVERA MONOBLOC M302 stretcher is a medical device intended for transporting a lying person both inside and outside the vehicle. It is designed for use by professional users. It is intended to be used in combination with a mattress and a safety belt system.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050199PATIENT TRANSFER STRETCHERS - 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

UDI-PI traceability

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Expiration date
Manufacturing date
Serial number
Software identification