WAVELIGHT REFRACTIVE SUITE

GUDID 00380659907463

REFRACTIVE SUITE SWIVEL BED

Alcon Laboratories, Inc.

Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered Ophthalmic chair, line-powered
Primary Device ID00380659907463
NIH Device Record Keyc1661a28-531f-4dae-9322-55e28041dc49
Commercial Distribution StatusIn Commercial Distribution
Brand NameWAVELIGHT REFRACTIVE SUITE
Version Model Number8065990746
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound
Weight800 Pound

Device Identifiers

Device Issuing AgencyDevice ID
GS100380659907463 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LZSExcimer Laser System

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2014-09-24

On-Brand Devices [WAVELIGHT REFRACTIVE SUITE]

00380659908965STAND ALONE PATIENT BED
00380659907463REFRACTIVE SUITE SWIVEL BED
00380659906060ALLEGRO ANALYZER. The WaveLight® Topolyzer™ VARIO and WaveLight® Analyzer II diagnostic devi
00380650001108STAND ALONE PATIENT BED

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.