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Implantable reinforcing felt for surgical applications CORTEX 1

by VUP Medical, a.s. Czech Republic EUDAMED

Ref 101-0406Model CORTEX 1 40x60mm

EMDN H900302

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08591954802823 Basic UDI-DIDate22 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Implantable reinforcing felt for surgical applications CORTEX
Model / Reference
CORTEX 1 40x60mm, 101-0406
Primary DI / UDI-DI
08591954802823
Basic UDI-DI
B-08591954802823
EMDN Code
H900302 Suture felts
Device Class
Class III
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000042015

Other devices from VUP Medical, a.s.

See all devices from VUP Medical, a.s. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 41bb37d1-90a9-418e-bdb3-2b3a85f52296 61 fields · synced 23 Oct 2026