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Medilon

by Medilon Braces 15 variants

Ref MB2304Model Medilon Corestab Buikband Maat S

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8720865045CORE-STABM3 Basic UDI-DI Date29 May 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Medilon
Medilon Braces
Model / Reference
Medilon Corestab Buikband Maat S, MB2304
Primary DI / UDI-DI
08720865045603, 08719327483442, 08720865045634, 08719327483435
Basic UDI-DI
8720865045CORE-STABM3
EMDN Code
Y060403 Abdominal muscles supports
Device Class
Class I
EU market of registration
Poland
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000047759

Other devices from Medilon Braces

See all devices from Medilon Braces →

Properties

Other properties (13)

  • Sterile: No
  • 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