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GRUPPO FARMAIMPRESA SRL

Italy Last updated 8 Jun 2026

Devices
322
Registries
EUDAMED
FDA recalls
0

Catalogue322

Page 1 of 7

Showing 1-50 of 322

EUDAMED certificates4

EUDAMED certificates (4)

ITALCERT SRL 0426 4 certificates

  • 021-00-06-MDR Supplemented

    Technical documentation EU MDR

    Issued
    29 Jul 2026
    Expires
    21 Jun 2028
    Reason
    Add device or group
  • 009-00-21-MDR Supplemented

    Quality management system EU MDR

    Issued
    6 Oct 2026
    Expires
    9 Jan 2028
    Reason
    Add device or group
  • 020-00-04-MDR Withdrawn

    Quality management system EU MDR

    Issued
    9 Jun 2025
    Expires
    21 Jun 2028
    Reason
    Other
  • 010-00-06-MDR Withdrawn

    Quality management system EU MDR

    Issued
    19 Jun 2024
    Expires
    9 Jan 2028
    Reason
    Other

Notified bodies

What GRUPPO FARMAIMPRESA SRL makes

Gruppo Farmaimpresa Srl manufactures oral and gastrointestinal solutions, including effervescent tablets (e.g., ALGIBABY SOD), antireflux medications (e.g., REFLUSEN L, REDIFLUX PRO), and suppositories (e.g., Clarogin ovuli). The portfolio also includes pediatric formulations like Simethicon Baby and eye drops (e.g., COMIL GTT), as well as prefilled syringes for intramuscular or subcutaneous administration (e.g., Introx 2%, Artox 2%). Additional products cover digestive aids (e.g., RILEFAST MAG) and liquid formulations for oral use (e.g., SYMETYCON w kroplach).

These devices are classified under EU regulations as Class IIa, Class IIb, and Class III, with all relevant products registered in the EUDAMED database. The manufacturer operates within the European Union, adhering to applicable medical device directives and regulations.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

How many devices does GRUPPO FARMAIMPRESA SRL have in the registry?

The registry currently lists 322 devices for GRUPPO FARMAIMPRESA SRL. Devices recorded under merged duplicate company entries are counted once.

Which registries list GRUPPO FARMAIMPRESA SRL's devices?

Among its 50 most recently registered devices, GRUPPO FARMAIMPRESA SRL has devices listed in EUDAMED (50 devices).

What risk classes do GRUPPO FARMAIMPRESA SRL's devices fall under?

Among its 50 most recently registered devices, the classes recorded for GRUPPO FARMAIMPRESA SRL's devices are Class IIa, Class IIb and Class III. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for GRUPPO FARMAIMPRESA SRL?

EUDAMED lists 4 certificates for GRUPPO FARMAIMPRESA SRL (quality management system; technical documentation) under MDR. The most recent was issued on 2026-10-06.

What are the newest devices from GRUPPO FARMAIMPRESA SRL in the registry?

The most recently registered devices listed for GRUPPO FARMAIMPRESA SRL include FILORIN, NEBIOS IPER, NARYBABY MONO IPER and BORAGYN 1%.

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

Information

Address
1, VIA CIPRO, BRESCIA, Italy
Phone
+39 800912951
EUDAMED SRN
IT-MF-000012625