Primary Device ID | 00380657530939 |
NIH Device Record Key | 52e7ee06-80e4-4ea0-81d6-7cc8947ef469 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ORA System® VerifEye™ |
Version Model Number | 8065753093 |
Company DUNS | 008018525 |
Company Name | Alcon Laboratories, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00380657530939 [Primary] |
NCF | Aberrometer, ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-08 |
Device Publish Date | 2020-08-31 |
00380659983283 | ORA System with VerifEyeTM+, Aberometer 190.5 |
00380657530939 | ORA System with VerifEyeTM+ 2.0, Cart |
00380657530038 | ORA System with VerifEyeTM Lynk, Cart |
00380657530014 | ORA System with VerifEyeTM Lynk, Aberrometer 195.5 |
00380657530007 | ORA System with VerifEyeTM Lynk, Aberrometer 190.5 |
00380657529995 | ORA System with VerifEyeTM Lynk, Aberrometer 184.5 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ORA SYSTEM 85419445 4262249 Live/Registered |
ALCON RESEARCH, LLC 2011-09-09 |