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Licellvi

by J world Co., Ltd. 93 variants

Ref JSFE-19-130L

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-08800047844177 Basic UDI-DI 08800047844177UDI-DIDate23 Jun 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  • Withdrawn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

Device Name
Sterile Single Use Absorbable Polydioxanone Suture with Needle
Model / Reference
JSFE-19-130L
Primary DI / UDI-DI
08800047844177
Basic UDI-DI
B-08800047844177
EMDN Code
H010101010104 Mounted polydioxanone monofilament with needle for tissue traction (‘barbed’)
Device Class
Class III
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
KR-MF-000026588
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from J world Co., Ltd.

See all devices from J world Co., 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