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Corelon

by Futura Surgicare Pvt Ltd

Ref FSPLPACORELON

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-FSPLPACORELONAD Basic UDI-DI D-FSPLPACORELONADUDI-DIDate10 Jul 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
FSPLPACORELON
Primary DI / UDI-DI
D-FSPLPACORELONAD
Basic UDI-DI
B-FSPLPACORELONAD
EMDN Code
H010201010101, H010201010102
Device Class
Class IIb
EU market of registration
Malta

Manufacturer details

EUDAMED SRN
IN-MF-000017571
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Futura Surgicare Pvt Ltd

See all devices from Futura Surgicare Pvt Ltd →

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