Fidia Farmaceutici S.p.A.

Certificate 40052

Rev. 2Supplemented

Valid until: Oct 24, 2029

Certificate 40052 is a valid Quality management system issued to Fidia Farmaceutici S.p.A. and registered in EUDAMED. Valid until October 24, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number: 40052
Certificate type: Quality management system
Certificate status: Supplemented
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0459400522

Validity

Issued: Jun 19, 2026
Valid from: Jun 19, 2026
Valid until: Oct 24, 2029

Manufacturer

Manufacturer: Fidia Farmaceutici S.p.A.
Manufacturer SRN: IT-MF-000026988
Manufacturer country: Italy

Notified body

Notified body
Notified body SRN: 0459
Notified body country: France

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile: Yes
Human tissues: No
Animal tissues: No
In vitro diagnostics: No
Initial registration: Yes
New device: No
Discard allowed: No
SSCP enabled: No
Mechanism of scrutiny: No
Intended medical purpose: No
SPP applicable

History

Status changes

Supplemented

Supersedes

40052SupplementedMar 27, 2026 → Oct 24, 2029

Predecessor certificate not registered in EUDAMED.

Scope coverage

Class III1

1 scope

Solution viscoélastique pour usage intra-articulaire. Viscoelastic solution for intra-articular use.
Class III

Documents

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