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Fingertip Pulse Oximeters

EUDAMED

Class IIa (EU MDR)

Ref XM-114

by JOYTECH Healthcare Co., Ltd.

Identity

Trade Name
Fingertip Pulse Oximeters EUDAMED
Device Name
Fingertip Pulse Oximeters EUDAMED
Model / Reference
XM-114 EUDAMED

Identifiers

Primary DI / UDI-DI
06970392215372 EUDAMED
Basic UDI-DI
6970392211XM000287 EUDAMED
Direct Marketing DI
06970392215372 EUDAMED
EMDN Code
Z1203020408 PULSE OXIMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Fingertip Pulse Oximeters by Joytech Healthcare 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-000006020
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 59cd902a-5b74-4304-b067-459f35bd6355 61 fields · synced Jun 19, 2026