SpO2 sensor

by Shenzhen Redy-Med Technology Co., Ltd 9 variants

Ref RD130F-29Model RD130F-29,RD130S-29

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-CN-MF-000029812TM Basic UDI-DI D-CN-MF-000029812TMUDI-DI	Date12 Sep 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: SpO2 sensor
Model / Reference: RD130F-29, RD130S-29

Primary DI / UDI-DI: D-CN-MF-000029812TM
Basic UDI-DI: B-CN-MF-000029812TM
EMDN Code: C900301 Pulse oximeter sensors

Device Class: Class IIb
EU market of registration: Portugal

Manufacturer details

EUDAMED SRN: CN-MF-000029812
Authorised representative: Umedwings Netherlands B.V. NL-AR-000000444

From the manufacturer

Manufacturer's product page: Spo2

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Properties

Measuring Function

Other properties (10)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Incorporates Medicinal Product: No