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Intensiv SA

CH-MF-000036274 · Switzerland · Montagnola

Intensiv SA is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa35

Authorised representative in the Union: Intensiv Trade GmbH.

Devices declared under this manufacturer

Showing 12 of 35 declared devices.

Catalogue references include AO2018DS/3, AO2018OS/3, DSMAO2018DS/3, DSMIPRDC100/3, IPR-DC050/3, PX4015/12.

European nomenclature codes declared: Q010499, Q010199, Q01010403.

United States market access

FDA establishment registerRegistered with FDA
Matched entryINTENSIV SA (CH) · FDA 8030958
Devices in EUDAMED35
Country of registrationSwitzerland

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryINTENSIV SA

North American profile: Both markets. Intensiv SA is registered in both the United States and Canada.

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