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Cereform®

by Euromi Biosciences Belgium EUDAMED

Ref RMMV375+

EMDN P0601010202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03664685004530 Basic UDI-DIDate6 May 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 23 Oct 2026

Device Name
Cereform® Silicone Gel-Filled Breast Implants
Model / Reference
RMMV375+
Primary DI / UDI-DI
03664685004530
Basic UDI-DI
B-03664685004530
EMDN Code
P0601010202 Breast implants, round, made of silicone, with textured surface
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
BE-MF-000020089

Other devices from Euromi Biosciences

See all devices from Euromi Biosciences →

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 e9368319-479c-4e59-a399-f198702a389c 61 fields · synced 23 Oct 2026