Aneroid sphygmomanometers

by Wenzhou Fengrui Medical Instrument Co., Ltd. 12 variants

Model FG-802, FR-01，FG-802，FG-803，AS102 or AS-102 (ASPEN)

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-06976530420028 Basic UDI-DI 06976530420028UDI-DI	Date17 May 2024Registered	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Withdrawn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: Aneroid sphygmomanometer
Model / Reference: FG-802, FR-01，FG-802，FG-803，AS102 or AS-102 (ASPEN)

Primary DI / UDI-DI: 06976530420028
Basic UDI-DI: B-06976530420028, 69765304210019D
EMDN Code: C9006 Aneroid sphygmomanometers

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: CN-MF-000036488
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

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Properties

Contains Latex
Measuring Function

Other properties (11)

Sterile: No
Implantable: No
Reusable: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Incorporates Medicinal Product: No