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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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LO.LI. PHARMA S.r.l.

Certificate IT339826

Rev. 1Issued
Valid until
Apr 15, 2029

Certificate IT339826 is a valid Quality management system issued to LO.LI. PHARMA S.r.l. and registered in EUDAMED. Valid until April 15, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
IT339826
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
1370IT3398261

Validity

Issued
Feb 6, 2025
Valid from
Feb 6, 2025
Valid until
Apr 15, 2029

Manufacturer

Manufacturer
LO.LI. PHARMA S.r.l.
Manufacturer SRN
IT-MF-000023734
Manufacturer country
Italy

Notified body

Notified body
BUREAU VERITAS ITALIA S.P.A.
Notified body SRN
1370
Notified body country
Italy

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
Yes
Intended medical purpose
No
SPP applicable
No
Conditions applicable
—
MOS outside EUDAMED
—
QMS/MOS type
Class IIb only

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIb2

2 scopes

  • Dispositivi per otorinolaringoiatria – Altri - MDN 1213 - Dispositivi non impiantabili non attivi costituiti da sostanze destinate a essere introdotte nel corpo umano attraverso un orifizio del corpo o per via cutanea
    Class IIb
  • BRONCOSITOL (10 FIALE, SAGGIO), EUSITOL (10 FIALE, SAGGIO), AEROSITOL (10 FIALE, SAGGIO)
    Class IIb

Documents

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