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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

EM153 — Class I MDR by SIMAD S.R.L.

MD Atlas
SIMAD S.R.L.

EUDAMED last updated this device on May 26, 2023

EM153

805714374VEDOGB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SIMAD S.R.L.
UDI-DI code: 08057143740067
Reference / catalog number: EM153

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View device family (Basic UDI)

Manufacturer information

Organization name: SIMAD S.R.L.
SRN: IT-MF-000027245
Manufacturer status: Active

Related devices

EMS F3H2 P805714374MOONRAYWFOn the market EMS F3H2 V805714374MOONRAYWFOn the market EMS F3H1 G805714374MOONRAYWFOn the market EMS F3H2 G805714374MOONRAYWFOn the market EMS F3H1 P805714374MOONRAYWFOn 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

2 warnings recorded — scroll inside the panel to see all entries.

CW016
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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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: 08057143740067
Basic UDI-DI: 805714374VEDOGB
Reference / catalog number: EM153
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: Il tavolo operatorio VEDO è un dispositivo medico attivo destinato a sostenere e posizionare il paziente durante interventi chirurgici. Movimenti eseguibili: traslazione longitudinale, trendelenburg, antitrendelenburg, salita/discesa, traslazione trasversale, inclinazione laterale (destra e sinistra)
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.

Z12011202OPERATING TABLES

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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