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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

978730613A — Class I MDR by Villa Sistemi Medicali…

MD Atlas
Villa Sistemi Medicali S.p.A.

EUDAMED last updated this device on Dec 4, 2024

978730613A

805773712FT2369T

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Villa Sistemi Medicali S.p.A.
UDI-DI code: 08057737123795
Reference / catalog number: 978730613A

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View device family (Basic UDI)

Manufacturer information

Organization name: Villa Sistemi Medicali S.p.A.
SRN: IT-MF-000016860
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

049/MDRIssued
Quality management systemNotified body: 0051Expiry: Oct 4, 2027

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: 08057737123795
Basic UDI-DI: 805773712FT2369T
Reference / catalog number: 978730613A
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: —
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.

Z11030503PATIENT TABLES FOR RADIOLOGICAL EQUIPMENT

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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