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S.c.a

EUDAMED

Class I (EU MDR)

Ref 20.471.01Model S.C.A

by Samsun Cerrahi̇ Aletler Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇

Identity

Trade Name
S.C.A EUDAMED
Device Name
CUTTER EUDAMED
Model / Reference
S.C.A EUDAMED
20.471.01 EUDAMED

Identifiers

Primary DI / UDI-DI
08698980491271 EUDAMED
Basic UDI-DI
868086255S.C.A3544TN EUDAMED
EMDN Code
L170401 CORNEAL TREPHINES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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

Category: Corneoscleral punch

S.c.a by Samsun Cerrahi̇ Aletler Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇ — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Corneoscleral punch.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000018747

Sources (1)

  • EUDAMED 22d8dfc1-5663-4ea9-b128-37a6f625275b 61 fields · synced Oct 1, 2026