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Kapátko oční ALFA

EUDAMED

Class I (EU MDR)

Ref 0228

by ALFA VITA, s.r.o.

Identity

Trade Name
Kapátko oční ALFA EUDAMED
Device Name
Kapátko oční ALFA EUDAMED
Model / Reference
0228 EUDAMED

Identifiers

Primary DI / UDI-DI
08594027312908 EUDAMED
Basic UDI-DI
859402731006GZ EUDAMED
Direct Marketing DI
08594027312908 EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Kapátko oční ALFA by ALFA VITA, s.r.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
ALFA VITA, s.r.o.
EUDAMED SRN
CZ-MF-000051941

Sources (1)

  • EUDAMED 698fff9f-548b-4b60-bf21-fceda943b5a7 61 fields · synced Jun 19, 2026