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Supintro

EUDAMED

Class III (EU MDR)

Ref 123456Model EHA102SUP

by Erc Bi̇yoteknoloji̇ San.ve Diş Ti̇c.aş.

Identity

Device Name
SUPINTRO EUDAMED
Model / Reference
EHA102SUP EUDAMED
123456 EUDAMED

Identifiers

Primary DI / UDI-DI
D-8681665500726B6 EUDAMED
Basic UDI-DI
B-8681665500726B6 EUDAMED
EMDN Code
P091399 ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - OTHER 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

Category: Joint prosthesis implantation kit, single-use

Supintro by Erc Bi̇yoteknoloji̇ San.ve Diş Ti̇c.aş. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Joint prosthesis implantation kit, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000027082

Sources (1)

  • EUDAMED b3387d64-6e3f-4e57-948f-8a724e13a5a4 61 fields · synced Jul 16, 2026