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E.P. Medica S.r.l.

Active in EUDAMED

Italyfrom SRN EUDAMED SRN IT-MF-000035449

Devices
25
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What E.P. Medica S.r.l. makes

E.P. Medica S.r.l. manufactures diagnostic and therapeutic kits (Kit K02 - D01) for medical procedures, nasal scraping devices, and nebuliser syringes (Siringa-NEB). Their portfolio includes rapid diagnostic tools like Nasir Rapid and Nasir for nasal sampling, as well as Alzalingua, a device likely used for linguistic or speech-related assessments. These products are designed for clinical and home-use applications.

The company’s devices are classified under EU Medical Device Regulations as Class I or Class IIa, indicating low to moderate risk. All listed products appear in the EU’s eudamed registry, ensuring traceability and compliance with European Union medical device directives. The manufacturer is based in Italy.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue25

Newest first, rows 1-25 of 25

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  • Kit K02 - D01 Ref G15

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref G06

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref G13

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref G14

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref G09

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K03

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K04

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K15

    Class IIa
    Active CE MDR EUDAMED IIa

  • Nasir Ref D02

    Class I
    Active CE MDR EUDAMED I

  • Kit K02 - D01 Ref K16

    Class IIa
    Active CE MDR EUDAMED IIa

  • Nasal Scraping Ref D11

    Class I
    Active CE MDR EUDAMED I

  • Kit K02 - D01 Ref K09

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K05

    Class IIa
    Active CE MDR EUDAMED IIa

  • Alzalingua Ref D04

    Class I
    Active CE MDR EUDAMED I

  • Siringa-NEB Ref A01

    Class I
    Active CE MDR EUDAMED I

  • Nasir Rapid Ref D07

    Class I
    Active CE MDR EUDAMED I

  • Nasir Ref D01

    Class I
    Active CE MDR EUDAMED I

  • Kit K02 - D01 Ref K06

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K07

    Class IIa
    Active CE MDR EUDAMED IIa

  • Nasir Baby Ref D05

    Class I
    Active CE MDR EUDAMED I

  • Nasir NEB Ref D10

    Class I
    Active CE MDR EUDAMED I

  • Nas-Air Ref D06

    Class I
    Active CE MDR EUDAMED I

  • Kit K02 - D01 Ref K14

    Class IIa
    Active CE MDR EUDAMED IIa

  • Kit K02 - D01 Ref K13

    Class IIa
    Active CE MDR EUDAMED IIa

Rows 1-25 of 25

Company details

EUDAMED SRN
IT-MF-000035449
SRN (system / procedure pack)
IT-PR-000041267
EU VAT number
02506400395
EUDAMED status
Active
EUDAMED registered name
E.P. Medica S.r.l.
Registered address
43/B, Via dell'Artigianato, 48034, Fusignano, Italy
Website
epmedica.it/
Phone
+3905451893255
PRRC contact
Eleonora Pollini(public in EUDAMED)

Frequently asked questions

How many devices does E.P. Medica S.r.l. have in the registry?

The registry currently lists 25 devices for E.P. Medica S.r.l.. Devices recorded under merged duplicate company entries are counted once.

Which registries list E.P. Medica S.r.l.'s devices?

Among its 25 most recently registered devices, E.P. Medica S.r.l. has devices listed in EUDAMED (25 devices).

What risk classes do E.P. Medica S.r.l.'s devices fall under?

Among its 25 most recently registered devices, the classes recorded for E.P. Medica S.r.l.'s devices are Class I and Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from E.P. Medica S.r.l. in the registry?

The most recently registered devices listed for E.P. Medica S.r.l. include Kit K02 - D01, Nasir, Nasal Scraping and Alzalingua.

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