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Yakebot

EUDAMED

Class IIa (EU MDR)

Ref CYK000000013Model DRS-02-RA-Pro

by Beijing Yakebot Technology Co., Ltd.

Identity

Trade Name
Yakebot EUDAMED
Device Name
Robotic device for detal implantology EUDAMED
Model / Reference
DRS-02-RA-Pro EUDAMED
CYK000000013 EUDAMED

Identifiers

Primary DI / UDI-DI
06975130760084 EUDAMED
Basic UDI-DI
697513076008JC EUDAMED
Direct Marketing DI
06975130760084 EUDAMED
EMDN Code
Z12011401 SURGICAL NAVIGATION SYSTEM EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Yakebot by Beijing Yakebot Technology 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-000038958
Authorised Representative
PureCE B.V. NL-AR-000006069

Sources (1)

  • EUDAMED 9a9ba18f-ba40-44a6-afad-4ba4636f7b73 61 fields · synced Jun 18, 2026