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Probe

EUDAMED

Class I (EU MDR)

Ref BFS000000028Model SA-02-MAK-02

by Beijing Yakebot Technology Co., Ltd.

Identity

Device Name
Probe EUDAMED
Model / Reference
SA-02-MAK-02 EUDAMED
BFS000000028 EUDAMED

Identifiers

Primary DI / UDI-DI
06975130760121 EUDAMED
Basic UDI-DI
697513076012J3 EUDAMED
EMDN Code
Q010599 DENTAL INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Malta 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Probe by Beijing Yakebot Technology Co., Ltd. — Class I — 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 6a9133bd-11c1-4361-b9a9-5e44d1a87dcd 61 fields · synced Jun 18, 2026