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Naviblef Daily Care

EUDAMED

Class I (EU MDR)

Ref F50ND

by Novax Pharma SAM

Identity

Trade Name
NAVIBLEF DAILY CARE EUDAMED
Device Name
NAVIBLEF DAILY CARE EUDAMED
Model / Reference
F50ND EUDAMED

Identifiers

Primary DI / UDI-DI
D-F50NDRM EUDAMED
Basic UDI-DI
B-F50NDRM EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Naviblef Daily Care by Novax Pharma SAM — Class I — 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
Novax Pharma SAM
EUDAMED SRN
MC-MF-000011256
Authorised Representative
International Associates Auditing & Certification Limited IE-AR-000002248

Sources (1)

  • EUDAMED d31a6f82-59e4-4173-8ef4-c7bf632b835b 61 fields · synced Jul 10, 2026