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Trial inlay S/M

EUDAMED

Class IIa (EU MDR)

Ref 02366064

by AQ Solutions GmbH

Identity

Trade Name
Trial inlay S/M EUDAMED
Device Name
Trial Implants EUDAMED
Model / Reference
02366064 EUDAMED

Identifiers

Primary DI / UDI-DI
04251704207387 EUDAMED
Basic UDI-DI
42517042003JT EUDAMED
Direct Marketing DI
04251704207387 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 inlay S/M 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 05a8bde0-b43d-4810-9131-4555ad1207a1 61 fields · synced Jun 18, 2026