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Sorbimesh

by Assut Europe SpA EUDAMED

Active European Union

Ref SM07P

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0013236626 Date28 Sep 2026IssuedStatusActive expires 7 Aug 2028

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0013236626 Supplemented

    Quality management system EU MDR

    Issued
    28 Sep 2026
    Expires
    7 Aug 2028
    Reason
    Add device or group
  • CVD003924 Issued

    Technical documentation EU MDR

    Issued
    4 Dec 2024
    Expires
    7 Aug 2028

Specification

EUDAMED

Model / Reference
SM07P
Primary DI / UDI-DI
08033439435091
Basic UDI-DI
8033439SORBIMESHT7
Direct Marketing DI
08033439435091
EMDN Code
P900204 Surgical meshes, more than one component
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000018178

Other devices from Assut Europe SpA

  • Filbloc

    Class III
  • Assufil

    Class III
  • Darvin Lac

    Class III
  • Assufil Monofilamento

    Class III
  • Monofil Fast

    Class III
  • Assunyl

    Class III

See all devices from Assut Europe SpA →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No