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Fascigel HA

by Contipro a.s. Czechia EUDAMED

Ref 160017 EMDN P9099

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859516379900NY Basic UDI-DIDate23 Jul 2025RegisteredStatusActive

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  • Withdrawn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)
  • 2025-MDR/QS-033 Issued

    Quality management system EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    10 Jul 2025
    Expires
    4 Aug 2028
  • 2025-MDR/TD-033 Issued

    Technical documentation EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    10 Jul 2025
    Expires
    4 Aug 2028

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
160017
Primary DI / UDI-DI
08595163799028
Basic UDI-DI
859516379900NY
EMDN Code
P9099 Implantable prosthetic devices - other
Device Class
Class III
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000014702

Other devices from Contipro a.s.

See all devices from Contipro a.s. →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED fb3bd5dd-a43a-416d-a5de-fbf799a9420a 61 fields · synced 22 Oct 2026