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Eumill Allergie

EUDAMED

Class IIb (EU MDR)

Ref EUALPLVN010FModel OC01

by Nirial Pharma srl

Identity

Trade Name
Eumill Allergie EUDAMED
Device Name
Ocular Drops EUDAMED
Model / Reference
OC01 EUDAMED
EUALPLVN010F EUDAMED

Identifiers

Primary DI / UDI-DI
08052990632268 EUDAMED
Basic UDI-DI
805299063OFTA001MA EUDAMED
EMDN Code
Q02030299 OPHTHALMOLOGY, LIQUID FLUIDS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

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

Eumill Allergie by Nirial Pharma srl — Class IIb — 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
Nirial Pharma srl
EUDAMED SRN
IT-MF-000018760

Sources (1)

  • EUDAMED 0ddb8f8d-8914-451d-8283-33e0217b9128 61 fields · synced Oct 6, 2026