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Optive

EUDAMED

Class IIb (EU MDR)

Ref 93304LT

by Allergan Sales, LLC

Identity

Trade Name
OPTIVE EUDAMED
Device Name
Dry Eye Comfort Solutions and Ointments EUDAMED
Model / Reference
93304LT EUDAMED

Identifiers

Primary DI / UDI-DI
10840228300899 EUDAMED
Basic UDI-DI
0840228300034F EUDAMED
Direct Marketing DI
10840228300899 EUDAMED
EMDN Code
Q02030206,Q02030299,Q0299 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Lithuania EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Optive by Allergan Sales, LLC — 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
Allergan Sales, LLC
EUDAMED SRN
US-MF-000001517
Authorised Representative
Allergan Pharmaceuticals International Limited IE-AR-000000650

Sources (1)

  • EUDAMED e0cca78e-d1be-48e8-954b-0940b7e4b53d 61 fields · synced Jun 18, 2026