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A-Aequa

EUDAMED

Class III (EU MDR)

Ref 0193122Model A-AEQUA REVISION CEMENTLESS STEM MEDIUM SIZE A 22 M

by Adler Ortho S.p.A

Identity

Trade Name
A-AEQUA EUDAMED
Model / Reference
A-AEQUA REVISION CEMENTLESS STEM MEDIUM SIZE A 22 M EUDAMED
0193122 EUDAMED

Identifiers

Primary DI / UDI-DI
08050880237258 EUDAMED
Basic UDI-DI
B-08050880237258 EUDAMED
EMDN Code
P090804030202 REVISION UNCEMENTED FEMORAL STEMS, WITH MODULAR NECK EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

A-Aequa by Adler Ortho S.p.A — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Adler Ortho S.p.A
EUDAMED SRN
IT-MF-000010164

Sources (1)

  • EUDAMED dc80d504-6ae7-43a6-ba81-59fcebb83850 61 fields · synced Oct 1, 2026