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Ethisorb

by Johnson & Johnson International Belgium EUDAMED

Ref EDP23S

EMDN M9099

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-BEMF000008018000017NN Basic UDI-DIDate4 Aug 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 24 Oct 2026

Model / Reference
EDP23S
Primary DI / UDI-DI
D-BEMF000008018000017NN
Basic UDI-DI
B-BEMF000008018000017NN
EMDN Code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000008018

Other devices from Johnson & Johnson International

See all devices from Johnson & Johnson International →

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 D-BEMF000008018000017NN|B-BEMF000008018000017NN 61 fields · synced 24 Oct 2026