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Wired Single Axis Electrogoniometer

EUDAMED

Class I (EU MDR)

Ref F35 Single Axis Electrogoniometer

by Biometrics Ltd

Identity

Trade Name
Wired Single Axis Electrogoniometer EUDAMED
Device Name
Data Acquisition Products EUDAMED
Model / Reference
F35 Single Axis Electrogoniometer EUDAMED

Identifiers

Primary DI / UDI-DI
05060481691307 EUDAMED
Basic UDI-DI
506048169DataAcqProdAD EUDAMED
EMDN Code
V030202 GONIOMETERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Wired Single Axis Electrogoniometer by Biometrics Ltd — Class I — 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

Manufacturer
Biometrics Ltd
EUDAMED SRN
GB-MF-000002774
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED e24cc06d-54a8-444a-8048-cdb7a9cdd1aa 61 fields · synced Jul 30, 2026