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Electronic Blood Pressure Monitor

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref JPD-HA120

by Shenzhen Jumper Medical Equipment Co., Ltd

Identity

Trade Name
Electronic Blood Pressure Monitor EUDAMED
JUMPER FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
Electronic Blood Pressure Monitor EUDAMED
Model / Reference
JPD-HA120 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06951740517720 EUDAMEDFDA UDI
Basic UDI-DI
69517405HA01NU EUDAMED
Direct Marketing DI
06951740517720 EUDAMED
FDA Product Code
DXN FDA UDI
EMDN Code
Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED
GMDN Term
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.1130 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Electronic Blood Pressure Monitor by Shenzhen Jumper Medical Equipment Co., Ltd — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

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

Sources (3)

  • EUDAMED 908a30df-9c42-4974-b101-164bd6cf63a1 61 fields · synced Oct 6, 2026
  • FDA UDI c9d9348b-8506-47e5-a2f9-1bf49ff57052 32 fields · synced May 30, 2026
  • FDA 510(k) K231310 1 fields · synced May 18, 2026