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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

000ARSX3P — Class I MDR by Multix solutions srl

MD Atlas
Multix solutions srl

EUDAMED last updated this device on Mar 23, 2026

000ARSX3P

++G035MULTIXSOLUTIONSBQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Multix solutions srl
UDI-DI code: G035000ARSX3P0
Reference / catalog number: 000ARSX3P

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Manufacturer information

Organization name: Multix solutions srl
SRN: IT-MF-000021627
Manufacturer status: Active

Related devices

X1-GT-77H-F++G035MULTIXSOLUTIONSBQOn the market 002ANDX1T++G035MULTIXSOLUTIONSBQOn the market 001ANDX1T++G035MULTIXSOLUTIONSBQOn the market 000ANDX2++G035MULTIXSOLUTIONSBQOn the market 002ANDX3P++G035MULTIXSOLUTIONSBQOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: G035000ARSX3P0
Basic UDI-DI: ++G035MULTIXSOLUTIONSBQ
Reference / catalog number: 000ARSX3P
Issuing entity: HIBCC

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: TROLLEY X3 PLUS
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.

V0880MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

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.