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ESTElift

by 21 Century Medical Co., Ltd. 57 variants

Ref DS26038050I

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-08809794023453 Basic UDI-DI 08809794023453UDI-DIDate12 Jul 2022RegisteredStatusActive

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  • Withdrawn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 polydioxanone Suture with needle
Model / Reference
DS26038050I
Primary DI / UDI-DI
08809794023453
Basic UDI-DI
B-08809794023453
EMDN Code
H010101010104 Mounted polydioxanone monofilament with needle for tissue traction (‘barbed’)
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000009204
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from 21 Century Medical Co., Ltd.

See all devices from 21 Century Medical 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