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ReDura

by Medprin Regenerative Medical Technologies Co., Ltd. China EUDAMED

Ref RDS-1205

EMDN P900399

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06953913601137 Basic UDI-DIDate18 Oct 2022RegisteredStatusActive

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

Device Name
Regenerative Dural Repair Patch
Model / Reference
RDS-1205
Primary DI / UDI-DI
06953913601137
Basic UDI-DI
B-06953913601137
EMDN Code
P900399 Tissue patches - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000012874
Authorised representative
Medprin Biotech GmbH DE-AR-000007892

Other devices from Medprin Regenerative Medical Technologies Co., Ltd.

See all devices from Medprin Regenerative Medical Technologies Co., Ltd. →

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 46bdd557-05bb-463f-9c91-ba775b716f89 61 fields · synced 24 Oct 2026