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TrueLife Oximeter X5 BT

EUDAMED

Class IIa (EU MDR)

Ref JPD-500F

by Shenzhen Jumper Medical Equipment Co., Ltd

Identity

Trade Name
TrueLife Oximeter X5 BT EUDAMED
Device Name
Pulse Oximeter EUDAMED
Model / Reference
JPD-500F EUDAMED

Identifiers

Primary DI / UDI-DI
06951740540452 EUDAMED
Basic UDI-DI
69517405SP01TL EUDAMED
Direct Marketing DI
06951740540452 EUDAMED
EMDN Code
Z1203020408 PULSE OXIMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

TrueLife Oximeter X5 BT by Shenzhen Jumper Medical Equipment 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

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Manufacturer

EUDAMED SRN
CN-MF-000014343
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED c4059cc4-2478-4d7d-82c8-a9572363d6ee 61 fields · synced Jul 8, 2026