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Ligafast

by Futura Surgicare Pvt Ltd

Ref FSPLPGLALIGAFAST

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FSPLPGLALIGAFASTKW Basic UDI-DI D-FSPLPGLALIGAFASTKWUDI-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

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
FSPLPGLALIGAFAST
Primary DI / UDI-DI
D-FSPLPGLALIGAFASTKW
Basic UDI-DI
B-FSPLPGLALIGAFASTKW
EMDN Code
H0101010299 Synthetic absorbable multifilament sutures - other
Device Class
Class III
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