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Clareon Vivity

FDA UDIEUDAMED

Class III (US FDA UDI)

Ref CCWET5.085

by Alcon Laboratories, Inc.

Identity

Trade Name
Clareon Vivity EUDAMEDFDA UDI
Generic Name
Posterior-chamber intraocular lens, pseudophakic FDA UDI
Device Name
Clareon Vivity Toric Extended Vision UV Absorbing IOL EUDAMED
CLAREON UVA VIVITY TORIC FDA UDI
Model / Reference
CCWET5.085 EUDAMED
CCWET5 FDA UDI
Description
CLAREON UVA VIVITY TORIC FDA UDI

Identifiers

Catalog Number
CCWET5.085 FDA UDI
Primary DI / UDI-DI
00380652505529 EUDAMEDFDA UDI
Basic UDI-DI
038065GMN000245HB EUDAMED
FDA Product Code
POE FDA UDI
EMDN Code
P030102100301 IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHOBIC ACRYLIC EUDAMED
GMDN Term
Posterior-chamber intraocular lens, pseudophakic FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class III FDA UDI
Regulation Number
886.3600 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Posterior-chamber intraocular lens, pseudophakic

Clareon Vivity by Alcon Laboratories, Inc. — Class III — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Posterior-chamber intraocular lens, pseudophakic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 33a3e02f-6248-43ee-a6e9-7f186756728b 35 fields · synced Oct 8, 2026
  • EUDAMED ee3cdfb5-fcfa-4333-8fcd-2964694ac212 61 fields · synced Oct 8, 2026