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Cereform®

by Euromi Biosciences EUDAMED

Active European Union

Ref CEREFORM

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-40100EX Basic UDI-DIDate18 Feb 2022RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Device Name
Cereform® Silicone Gel-Filled Breast Implants
Model / Reference
CEREFORM
Primary DI / UDI-DI
D-40100EX
Basic UDI-DI
B-40100EX
EMDN Code
P0601010201 Breast implants, round, made of silicone, with smooth surface
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000020089

Other devices from Euromi Biosciences

See all devices from Euromi Biosciences →

Properties

  • 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