Skip to content

Eparina sodica S.A.L.F.

by S.A.L.F. S.p.A. Laboratorio Farmacologico 3 variants

Ref EESN.520GPO

Active European Union

CE MDR

Valid until

19 Jan 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0004231724 Date29 Apr 2026IssuedStatusActive expires 19 Jan 2028

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0004231724 Active Supplemented

    Quality management system EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    29 Apr 2026
    Expires
    19 Jan 2028
    Reason
    Change approved
  • CVD00240124 Active

    Technical documentation EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    19 Feb 2024
    Expires
    19 Jan 2028

Coverage

1 jurisdiction

Italy
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Italy

Specification

EUDAMED

Model / Reference
EESN.520GPO
Primary DI / UDI-DI
08052742103732
Basic UDI-DI
805274210SolEpaZ8
Unit of Use DI
18052742103739
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010720

Other devices from S.A.L.F. S.p.A. Laboratorio Farmacologico

See all devices from S.A.L.F. S.p.A. Laboratorio Farmacologico →

Properties

  • Sterile
  • Animal Tissues
  • Incorporates Medicinal Product

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No