← Back to catalogue

SZcaremed

EUDAMED

Class IIb (EU MDR)

Ref C310-21P

by Shenzhen Caremed Medical Technology Co., Ltd.

Identity

Trade Name
SZcaremed EUDAMED
Device Name
SpO2 Sensor EUDAMED
Model / Reference
C310-21P EUDAMED

Identifiers

Primary DI / UDI-DI
06931973429885 EUDAMED
Basic UDI-DI
B-06931973429885 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

SZcaremed by Shenzhen Caremed Medical Technology Co., Ltd. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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

Manufacturer

EUDAMED SRN
CN-MF-000010579
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 12ea0c16-29b8-4e9e-877b-64b91a282d9a 61 fields · synced Oct 8, 2026