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Myriad Matrix Soft Tissue Bioscaffold

by Aroa Biosurgery Ltd. 6 variants

Ref SR03LG1020WC

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-09421906017809 Basic UDI-DI 09421906017809UDI-DIDate22 Mar 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Myriad Matrix Soft Tissue Bioscaffold
Model / Reference
SR03LG1020WC
Primary DI / UDI-DI
09421906017809
Basic UDI-DI
B-09421906017809
EMDN Code
M04041001 Animal-derived collagen dressings, non-combined
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
NZ-MF-000003726
Authorised representative
S4M EUROPE FR-AR-000000180

Other devices from Aroa Biosurgery

See all devices from Aroa Biosurgery →

Properties

  • Sterile
  • Animal Tissues

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No