← Back to catalogue

VE liner

EUDAMED

Class III (EU MDR)

Ref C20050FModel JX 320 / 50

by Beijing LiDaKang Technology Co., Ltd.

Identity

Device Name
VE liner EUDAMED
Model / Reference
JX 320 / 50 EUDAMED
C20050F EUDAMED

Identifiers

Primary DI / UDI-DI
06942494999818 EUDAMED
Basic UDI-DI
B-06942494999818 EUDAMED
EMDN Code
P090803040101 STANDARD POLYETHYLENE HIP PROSTHESES INSERTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Non-constrained polyethylene acetabular liner

VE liner by Beijing LiDaKang Technology Co., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000027201
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED a5d3175b-4172-45a3-af47-b5ebfdf6f8b1 61 fields · synced Jul 9, 2026