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Quick Release Twin Tube

EUDAMED

Class I (EU MDR)

Ref I/ASS 8020F

by Medivance Instruments Limited

Identity

Trade Name
Quick Release Twin Tube EUDAMED
Device Name
AquaCare Components EUDAMED
Model / Reference
I/ASS 8020F EUDAMED

Identifiers

Primary DI / UDI-DI
50602095803334 EUDAMED
Basic UDI-DI
506020958AquaCareCIWF EUDAMED
EMDN Code
Q010199 CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Quick Release Twin Tube by Medivance Instruments Limited — 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

EUDAMED SRN
GB-MF-000024293
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 065df5e7-0d06-4d45-9c3e-0d150f6f0bd4 61 fields · synced Jun 19, 2026