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Serilia™

by ZooBiotic Ltd EUDAMED

Active European Union

Ref BM004

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5061104050006M3 Basic UDI-DIDate17 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
SERILIA™ Wound Matrix
Model / Reference
BM004
Primary DI / UDI-DI
50611040500204
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
UK-MF-000050361
Authorised representative
Dr. Ebeling & Assoc. GmbH DE-AR-000000003

Related devices

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Other devices from ZooBiotic Ltd