Purepoint

GUDID 00380657529872

Purepoint Laser

Alcon Laboratories, Inc.

Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope Indirect binocular laser ophthalmoscope
Primary Device ID00380657529872
NIH Device Record Key61ee4a45-a29b-42e6-951f-84ffb397f935
Commercial Distribution StatusIn Commercial Distribution
Brand NamePurepoint
Version Model Number8065752987
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

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
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
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
GS100380657529872 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HQFLaser, ophthalmic

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 Date2018-01-30

On-Brand Devices [Purepoint]

00380657529872Purepoint Laser
00380657505975PUREPOINT LASER SYSTEM
00380657515028PUREPOINT Laser 532nm Optical Laser Filter

Trademark Results [Purepoint]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PUREPOINT
PUREPOINT
88235379 not registered Live/Pending
John S. Dull & Associates, Inc.
2018-12-19
PUREPOINT
PUREPOINT
86733035 5200704 Live/Registered
MUFG Union Bank, National Association
2015-08-21
PUREPOINT
PUREPOINT
79124141 4457020 Live/Registered
Purepoint Holding B.V.
2012-12-04
PUREPOINT
PUREPOINT
78970656 not registered Dead/Abandoned
Edwards Lifesciences Corporation
2006-09-08
PUREPOINT
PUREPOINT
77214815 3459179 Live/Registered
NOVARTIS AG
2007-06-25
PUREPOINT
PUREPOINT
77036405 3462990 Live/Registered
NOVARTIS AG
2006-11-03
PUREPOINT
PUREPOINT
75977347 2181576 Live/Registered
PurePoint Filtration Systems, Inc.
1996-12-11
PUREPOINT
PUREPOINT
75976845 2153153 Live/Registered
PUREPOINT FILTRATION SYSTEMS, INC.
1995-05-26
PUREPOINT
PUREPOINT
75211572 not registered Dead/Abandoned
PurePoint Filtration Systems, Inc.
1996-12-11
PUREPOINT
PUREPOINT
74680194 not registered Dead/Abandoned
EFCO, Inc.
1995-05-26
PUREPOINT
PUREPOINT
74664198 not registered Dead/Abandoned
EFCO, Inc.
1995-04-21

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