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Quadrant FiniSense

EUDAMED

Class IIa (EU MDR)

Ref FS10Model Quadrant Systems

by Cavex Holland BV

Identity

Trade Name
Quadrant FiniSense EUDAMED
Device Name
Quadrant FiniSense EUDAMED
Model / Reference
Quadrant Systems EUDAMED
FS10 EUDAMED

Identifiers

Primary DI / UDI-DI
E241FS100 EUDAMED
Basic UDI-DI
++E241FS107E EUDAMED
EMDN Code
Q019008 DENTINAL DESENSITISERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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

Quadrant FiniSense by Cavex Holland BV — Class IIa — 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
Cavex Holland BV
EUDAMED SRN
NL-MF-000000423

Sources (1)

  • EUDAMED 60ec9992-a0c5-4051-b716-3812c2746898 61 fields · synced Aug 1, 2026