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Agilis

EUDAMED

Class III (EU MDR)

Ref 0700003Model AGILIS TI-POR CUP CENTRAL HOLE PLUG H 2 mm

by Adler Ortho S.p.A

Identity

Trade Name
AGILIS EUDAMED
Model / Reference
AGILIS TI-POR CUP CENTRAL HOLE PLUG H 2 mm EUDAMED
0700003 EUDAMED

Identifiers

Primary DI / UDI-DI
08052532832095 EUDAMED
Basic UDI-DI
B-08052532832095 EUDAMED
EMDN Code
P09088099 HIP PROSTHESES - OTHER ACCESSORIES 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 a5ef66d7-dc3c-4e0b-882a-323c9a652906 61 fields · synced Oct 6, 2026