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Alfasigma S.p.A.

Active in EUDAMED

Italyfrom SRN EUDAMED SRN IT-MF-000017931

Devices
2
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Alfasigma S.p.A. makes

Alfasigma S.p.A. makes medical devices such as negative-pressure wound therapy system foam dressings and ear drops like DEBROX GOCCE AURICOLARI, as well as products for herpes treatment like HERPESUN DEFEND.

The company's portfolio is classified as Class IIa devices and is listed in the eudamed registry, with the company based in Italy.

AI-generated from registry data, 27 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Debrox Gocce Auricolari Ref TFDM001

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Herpesun Defend Ref TFDM002

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa

Company details

EUDAMED SRN
IT-MF-000017931
EU VAT number
03432221202
EUDAMED status
Active
EUDAMED registered name
Alfasigma S.p.A.
EUDAMED abbreviated name
Alfasigma S.p.A.
Registered address
5, Via Ragazzi del '99, 40133, Bologna, Italy
Phone
+390516489511
PRRC contact
Elisabetta Beltrami(public in EUDAMED)

Frequently asked questions

How many devices does Alfasigma S.p.A. have in the registry?

The registry currently lists 2 devices for Alfasigma S.p.A.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Alfasigma S.p.A.'s devices?

Among its 2 most recently registered devices, Alfasigma S.p.A. has devices listed in EUDAMED (2 devices).

What risk classes do Alfasigma S.p.A.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Alfasigma S.p.A.'s devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Alfasigma S.p.A. in the registry?

The most recently registered devices listed for Alfasigma S.p.A. include DEBROX GOCCE AURICOLARI and HERPESUN DEFEND.

Generated automatically from registry data and not verified by a human reviewer.