← Back to catalogue

Fingertip Pulse Oximeter

EUDAMED

Class IIa (EU MDR)

Ref XM-113

by JOYTECH Healthcare Co., Ltd.

Identity

Trade Name
Fingertip Pulse Oximeter EUDAMED
Device Name
Fingertip Pulse Oximeters EUDAMED
Model / Reference
XM-113 EUDAMED

Identifiers

Primary DI / UDI-DI
06942284610848 EUDAMED
Basic UDI-DI
6970392211XM000287 EUDAMED
Direct Marketing DI
06942284610848 EUDAMED
EMDN Code
Z1203020408 PULSE OXIMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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 Oximeter 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000006020
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 282559fc-a262-4368-b565-8a9a58249e31 61 fields · synced Jun 19, 2026