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SeriliaTM

by ZooBiotic Ltd United Kingdom EUDAMED

Ref BM003 EMDN M040499

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  • Withdrawn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 · synced 24 Oct 2026

Device Name
SERILIA™ Wound Matrix
Model / Reference
BM003
Primary DI / UDI-DI
50611040500136
Basic UDI-DI
5061104050006M3
EMDN Code
M040499 Dressings for wounds, sores and ulcerations - other
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

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

Other devices from ZooBiotic Ltd

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • Implantable: No
  • 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 49628c44-572b-4341-8f3c-5353d12e1b6c 61 fields · synced 24 Oct 2026