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Ultra V Ez Cannula

EUDAMED

Class III (EU MDR)

Ref LF19100200CRef PCJL19100200A

by 21 Century Medical Co., Ltd.

Identity

Trade Name
Ultra V Ez Cannula EUDAMED
Ultra V Ez Cannula L PDO MOLD COG Ⅱ EUDAMED
Device Name
Sterile single use polydioxanone Suture with needle EUDAMED
Model / Reference
LF19100200C EUDAMED
PCJL19100200A EUDAMED

Identifiers

Primary DI / UDI-DI
08809822316502 EUDAMED
08809822318186 EUDAMED
Basic UDI-DI
B-08809822316502 EUDAMED
B-08809822318186 EUDAMED
EMDN Code
H010101010104 MOUNTED POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR TISSUE TRACTION (‘BARBED’) EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Belgium EUDAMED
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ultra V Ez Cannula by 21 Century Medical Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 5699b56f-65ca-4835-9767-fbdc6500cefb 61 fields · synced Jul 22, 2026
  • EUDAMED c2da0d83-909c-4a9c-b566-767163821ec2 61 fields · synced May 18, 2026