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Agilis

EUDAMED

Class III (EU MDR)

Ref 0758142Model AGILIS Ti-Por CUP SIZE 42 for 32 mm HEAD

by Adler Ortho S.p.A

Identity

Trade Name
AGILIS EUDAMED
Model / Reference
AGILIS Ti-Por CUP SIZE 42 for 32 mm HEAD EUDAMED
0758142 EUDAMED

Identifiers

Primary DI / UDI-DI
08052532833672 EUDAMED
Basic UDI-DI
B-08052532833672 EUDAMED
EMDN Code
P0908030601 PRE-ASSEMBLED ACETABULAR COMPONENTS WITH CERAMIC INSERT 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

Agilis 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 2987c956-e5d6-4b30-8eb9-6ad6e8573184 61 fields · synced Aug 4, 2026