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Optomesh ULTRALIGHT

by Tricomed S.A. Poland EUDAMED

Ref MB-271-OPUM-023Model M-Pore 300x450 mm

EMDN P900202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05906146504462 Basic UDI-DIDate28 May 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 22 Oct 2026

Model / Reference
M-Pore 300x450 mm, MB-271-OPUM-023
Primary DI / UDI-DI
05906146504462
Basic UDI-DI
B-05906146504462
EMDN Code
P900202 Polypropylene surgical meshes
Device Class
Class IIb
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000002483

From the manufacturer

Manufacturer's product page: Optomesh® ULTRALIGHT

Other devices from Tricomed S.A.

See all devices from Tricomed S.A. →

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 73065d92-5082-45aa-8ee7-97983042cc58 61 fields · synced 22 Oct 2026