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Trial cup M standard

EUDAMED

Class IIa (EU MDR)

Ref 02003048

by AQ Solutions GmbH

Identity

Trade Name
Trial cup M standard EUDAMED
Device Name
Trial Implants EUDAMED
Model / Reference
02003048 EUDAMED

Identifiers

Primary DI / UDI-DI
04251704209312 EUDAMED
Basic UDI-DI
42517042003JT EUDAMED
Direct Marketing DI
04251704209312 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Trial cup M standard by AQ Solutions GmbH — 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
AQ Solutions GmbH
EUDAMED SRN
DE-MF-000005306

Sources (1)

  • EUDAMED f73017a6-b29c-4479-954b-7d9264f3804c 61 fields · synced Jun 19, 2026