Elastic UV-Absorbing Silicone Posterior Chamber Intraocular Lens - Toric Optic

GUDID 00841542100533

Diopter: 28.5 SE/2.0 Toric; Overall Diameter (Length): 10.8 mm

STAAR SURGICAL COMPANY

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 ID00841542100533
NIH Device Record Key5d45f9d3-33a3-4f9a-be9d-2c03f677a8f7
Commercial Distribution StatusIn Commercial Distribution
Brand NameElastic UV-Absorbing Silicone Posterior Chamber Intraocular Lens - Toric Optic
Version Model NumberAA4203TF
Company DUNS054751110
Company NameSTAAR SURGICAL COMPANY
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 Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100841542100533 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MJPLens, Intraocular, Toric Optics

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-20

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