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Optava Advance

EUDAMED

Class IIb (EU MDR)

Ref 96465EKRef 96615EM

by Allergan Sales, LLC

Identity

Trade Name
OPTAVA ADVANCE EUDAMED
Device Name
Dry Eye Comfort Solutions and Ointments EUDAMED
Model / Reference
96465EK EUDAMED
96615EM EUDAMED

Identifiers

Primary DI / UDI-DI
10840228302206 EUDAMED
10840228301971 EUDAMED
Basic UDI-DI
0840228300034F EUDAMED
Direct Marketing DI
10840228302206 EUDAMED
10840228301971 EUDAMED
EMDN Code
Q02030206,Q02030299,Q0299 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain 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

Optava Advance 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 (2)

  • EUDAMED 0d994e09-5ee8-4b94-ad61-76c4ba676f85 61 fields · synced Jul 27, 2026
  • EUDAMED d2c3d286-99d7-4a01-a3fb-1920946f5bca 61 fields · synced May 18, 2026