← Back to catalogue

TrueLife Pulse2

EUDAMED

Class IIa (EU MDR)

Ref DBP-1333

by JOYTECH Healthcare Co., Ltd.

Identity

Trade Name
TrueLife Pulse2 EUDAMED
Device Name
Blood Pressure Monitor EUDAMED
Model / Reference
DBP-1333 EUDAMED

Identifiers

Primary DI / UDI-DI
06942284616116 EUDAMED
Basic UDI-DI
6970392211BP0001Y5 EUDAMED
Direct Marketing DI
06942284616116 EUDAMED
EMDN Code
Z1203020501 NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES 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 Pulse2 by Joytech Healthcare 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

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

Manufacturer

EUDAMED SRN
CN-MF-000006020
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED e4179be1-9268-42f5-870d-afd7f3f6c413 61 fields · synced Jul 12, 2026