← Back to catalogue

Trial condylar replacement

EUDAMED

Class IIa (EU MDR)

Ref 70300153Ref 70300159

by AQ Solutions GmbH

Identity

Trade Name
Trial condylar replacement EUDAMED
Device Name
Trial Implants EUDAMED
Model / Reference
70300153 EUDAMED
70300159 EUDAMED

Identifiers

Primary DI / UDI-DI
04251704209763 EUDAMED
04251704209770 EUDAMED
Basic UDI-DI
42517042003JT EUDAMED
Direct Marketing DI
04251704209763 EUDAMED
04251704209770 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 condylar replacement 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AQ Solutions GmbH
EUDAMED SRN
DE-MF-000005306

Sources (2)

  • EUDAMED 5e392304-b4ca-40aa-8fb2-3129fae0a607 61 fields · synced Jul 16, 2026
  • EUDAMED 86478e2b-4693-4efe-8517-816f53ae61bb 61 fields · synced May 17, 2026