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Gruppo Farmaimpresa SRL

Active in EUDAMED

Italyfrom SRN EUDAMED SRN IT-MF-000012625

Devices
322
Registrations
EUDAMED

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.

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

Catalogue322

Newest first, rows 301-322 of 322

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  • Acid-Eaze Plus Ref FT.CE.107.FA.5.12

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • COMIL GTT 100 ml Ref FT.MDR.16.8.100

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Repalgin Ref FT.CE.107.FG.7.24

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • Rilefast Ace Ref FT.MDR.26.13

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Reflusod Ref FT.CE.107.FH.2.300

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Canditon HA Ref FT.CE.111.FB.8

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • RILEFAST CE Spray Ref FT.MDR.26.SP

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Secol 100 Ml Ref FT.MDR.16

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Stomachon Spasm Ref FT.MDR.16

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • gasimetin simetikon kapi 0+ Ref FT.MDR.16

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Reflusen Plus L Ref FT.CE.107.FA.7.12

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Reflu Mag Ref FT.CE.107.2.12.LWN

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • Reflu Mag Lite Ref FT.CE.107.FG.18.12

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • Repalgin Ref FT.CE.107.FG.7.12

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • Caregyn Ref FT.CE.111

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • Nurse Harvey's 20 ml Ref FT.MDR.26

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Proreva Ref FT.CE.120.3

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Caregyn ovules Ref FT.CE.111.FB.2.IMT

    Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
  • RILEFAST CE 20 ml Ref FT.MDR.26

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Balatus 150 ml Ref FT.CE.108

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Reflusen Plus M Ref FT.CE.107.FA.6.12

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

Rows 301-322 of 322

Showing 301-322 of 322

Company details

EUDAMED SRN
IT-MF-000012625
SRN (system / procedure pack)
IT-PR-000036632
EU VAT number
05534151211
EUDAMED status
Active
EUDAMED registered name
GRUPPO FARMAIMPRESA SRL
Registered address
1, VIA CIPRO, 25124, BRESCIA, Italy
PRRC contact
DANIELE SCETTA(public in EUDAMED)

EUDAMED certificates4

4 certificates2 valid, 0 expired, 2 withdrawn or suspendedMDR 4next expiry 9 Jan 2028

EUDAMED certificates (4)

ITALCERT SRL 0426 4 certificates

  • 021-00-06-MDR Active Supplemented

    Technical documentation EU MDR

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