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880uv

EUDAMED

Class IIb (EU MDR)

Ref 880UVModel 880UV Aspheric

by U.S. IOL, Inc.

Identity

Device Name
880UV EUDAMED
Model / Reference
880UV Aspheric EUDAMED
880UV EUDAMED

Identifiers

Primary DI / UDI-DI
00814106016359 EUDAMED
Basic UDI-DI
B-00814106016359 EUDAMED
EMDN Code
P030102090201 IOLs, APHAKIC, MONOFOCAL, ASPHERIC, HYDROPHOBIC ACRYLIC EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Norway EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

880uv by U.S. Iol, Inc. — Class IIb — 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
U.S. IOL, Inc.
EUDAMED SRN
US-MF-000030660
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 1551593c-ebce-4a6d-8572-ed3c2de7a198 61 fields · synced Jul 29, 2026