← Back to catalogue

Wrist Electronic Blood Pressure Monitor

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref FC-BP220Model FC-BP200, FC-BP201, FC-BP210, FC-BP211, FC-BP220, FC-BP221

by Shenzhen Finicare Co., Ltd.

Identity

Trade Name
Wrist Electronic Blood Pressure Monitor EUDAMED
Finicare FDA UDI
Generic Name
Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Device Name
Wrist Electronic Blood Pressure Monitor EUDAMED
Model / Reference
FC-BP200, FC-BP201, FC-BP210, FC-BP211, FC-BP220, FC-BP221 EUDAMED
FC-BP220 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
06971522820374 EUDAMEDFDA UDI
Basic UDI-DI
697152282WEBP1LL EUDAMED
510(k) Number
K231367 FDA UDI
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Wrist Electronic Blood Pressure Monitor by Shenzhen Finicare Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
CN-MF-000024364
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED 12eaa631-9547-4cbe-9d87-df769a48093b 61 fields · synced Jun 1, 2026
  • FDA UDI aa42efbb-9b1a-49f3-bc84-14ab6ce46bbc 33 fields · synced May 30, 2026