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Sp7119

EUDAMED

Class IIb (EU MDR)

Ref 07-10-00Model SP7119

by Shenzhen SINO-K Medical Technology Co., Ltd.

Identity

Trade Name
SP7119 EUDAMED
Device Name
SPO2 Sensor EUDAMED
Model / Reference
SP7119 EUDAMED
07-10-00 EUDAMED

Identifiers

Primary DI / UDI-DI
06972820960571 EUDAMED
Basic UDI-DI
B-06972820960571 EUDAMED
EMDN Code
C900301 PULSE OXIMETER SENSORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Pulse oximeter probe, single-use

Sp7119 by Shenzhen SINO-K Medical Technology Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000021157
Authorised Representative
Prolinx GmbH DE-AR-000005129

Sources (1)

  • EUDAMED 70d73df9-b190-45c4-bb9e-4afc786d652b 61 fields · synced Jun 18, 2026