AcrySof™ IQ Vivity™ DAT015.220

GUDID 00380652424677

Sterile UV Absorbing Acrylic Foldable Aspheric Wavefront-Shaping Posterior Chamber Intraocular Lens

Alcon Laboratories, Inc.

Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic Posterior-chamber intraocular lens, pseudophakic
Primary Device ID00380652424677
NIH Device Record Keya71f11f0-6bfb-49fe-9549-639d1765f59f
Commercial Distribution StatusIn Commercial Distribution
Brand NameAcrySof™ IQ Vivity™
Version Model NumberDAT015
Catalog NumberDAT015.220
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com
Phone+1(800)862-5266
Emailweb.masterus@alcon.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]
GS100380652424677 [Primary]

FDA Product Code

POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens
POEExtended depth of focus intraocular lens

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-23
Device Publish Date2020-06-15

On-Brand Devices [AcrySof™ IQ Vivity™]

00380652427944Sterile UV Absorbing Acrylic Foldable Aspheric Wavefront-Shaping Toric Posterior Chamber Intraoc
00380652424677Sterile UV Absorbing Acrylic Foldable Aspheric Wavefront-Shaping Posterior Chamber Intraocular L

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