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Biopsy Instrument

EUDAMED

Class IIa (EU MDR)

Ref BC1101Model BC1101, KMC-015-10

by Shanghai Kinetic Medical Co., Ltd.

Identity

Trade Name
Biopsy Instrument EUDAMED
Device Name
Biopsy Instrument EUDAMED
Model / Reference
BC1101, KMC-015-10 EUDAMED
BC1101 EUDAMED

Identifiers

Primary DI / UDI-DI
06938695501165 EUDAMED
Basic UDI-DI
69386955BCJP EUDAMED
Direct Marketing DI
06938695501165 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

Biopsy Instrument 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 8fd83768-470e-475f-a4dd-52ad017b9dad 61 fields · synced Jun 19, 2026