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Corepd

by Futura Surgicare Pvt Ltd

Ref FSPLPDSCOREPD

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-FSPLPDSCOREPDFY Basic UDI-DI D-FSPLPDSCOREPDFYUDI-DIDate9 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

LithuaniaPolandRomaniaMalta
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

EU market availability

Made available in 4 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Lithuania since 10 Sep 2026
  • Malta since 10 Sep 2026
  • Poland since 10 Sep 2026
  • Romania since 10 Sep 2026

Last checked 31 Oct 2026.

Specification

EUDAMED

Model / Reference
FSPLPDSCOREPD
Primary DI / UDI-DI
D-FSPLPDSCOREPDFY
Basic UDI-DI
B-FSPLPDSCOREPDFY
EMDN Code
H010101010101, H010101010103
Device Class
Class III
EU market of registration
Lithuania

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