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Naviblef Tto Intensive Care

EUDAMED

Class IIa (EU MDR)

Ref F50NTTI

by Novax Pharma SAM

Identity

Trade Name
NAVIBLEF TTO INTENSIVE CARE EUDAMED
Device Name
NAVIBLEF TTO INTENSIVE CARE EUDAMED
Model / Reference
F50NTTI EUDAMED

Identifiers

Primary DI / UDI-DI
D-F50NTTIPG EUDAMED
Basic UDI-DI
B-F50NTTIPG EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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 Tto Intensive Care by Novax Pharma SAM — Class IIa — 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 d50c86b0-b597-4a96-9aaa-63fb90464335 61 fields · synced Jun 17, 2026