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Balloon Catheter

EUDAMED

Class IIa (EU MDR)

Ref LC102-2520Model LC102-2515, LC102-2520, LC102-2525, LC112-2515, LC112-2520, LC112-2525, LC103-2515, LC103-2520, LC103-2525, LC113-2515, LC113-2520, LC113-2525, SC112-2015, SC112-2020, SC112-2025, KMC-005-15, KMC-005-20, KMC-005-25

by Shanghai Kinetic Medical Co., Ltd.

Identity

Device Name
Balloon Catheter EUDAMED
Model / Reference
LC102-2515, LC102-2520, LC102-2525, LC112-2515, LC112-2520, LC112-2525, LC103-2515, LC103-2520, LC103-2525, LC113-2515, LC113-2520, LC113-2525, SC112-2015, SC112-2020, SC112-2025, KMC-005-15, KMC-005-20, KMC-005-25 EUDAMED
LC102-2520 EUDAMED

Identifiers

Primary DI / UDI-DI
06938695537133 EUDAMED
Basic UDI-DI
69386955FBJZ EUDAMED
Direct Marketing DI
06938695537133 EUDAMED
EMDN Code
P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

Balloon Catheter by Shanghai Kinetic Medical Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000017688
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED cf4301d7-61b3-4b44-bdb9-c5cf38b5621c 61 fields · synced May 22, 2026