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SZcaremed

EUDAMED

Class IIb (EU MDR)

Ref C403F-117

by Shenzhen Caremed Medical Technology Co., Ltd.

Identity

Trade Name
SZcaremed EUDAMED
Device Name
SpO2 Sensor EUDAMED
Model / Reference
C403F-117 EUDAMED

Identifiers

Primary DI / UDI-DI
06931973429939 EUDAMED
Basic UDI-DI
B-06931973429939 EUDAMED
EMDN Code
C900301 PULSE OXIMETER SENSORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

SZcaremed by Shenzhen Caremed 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-000010579
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 7527d636-308b-470e-b5e1-8edf2237c943 61 fields · synced Jun 18, 2026