Alcon, Coherent

GUDID 10380650102031

2 GA Curved Laser Probe

Alcon Laboratories, Inc.

Ophthalmic laser system beam guide
Primary Device ID10380650102031
NIH Device Record Key31fe3f9a-4fbc-47aa-bf80-4916f54173d5
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlcon, Coherent
Version Model Number8065010203
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 Numberfalse
Manufacturing Datefalse
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100380650102034 [Primary]
GS110380650102031 [Package]
Contains: 00380650102034
Package: Box [6 Units]
In Commercial Distribution

FDA Product Code

HQFLaser, ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-24

On-Brand Devices [Alcon, Coherent]

1038065750803423 GA Straight Laser Probe
1038065750133225 GA Straight Laser Probe
1038065010419620 GA Straight Illuminated Laser Probe
1038065010403520 GA Curved Illuminated Laser Probe
1038065010219220 GA Straight Laser Probe
103806501020312 GA Curved Laser Probe

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