LightLas 810

GUDID 04712826770635

LIGHTMED CORPORATION

Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system, photocoagulation/photostimulation Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system Ophthalmic solid-state laser system
Primary Device ID04712826770635
NIH Device Record Keyc7f3d7c4-1937-4848-8c1e-b8c9d12c2e0b
Commercial Distribution StatusIn Commercial Distribution
Brand NameLightLas 810
Version Model NumberLD0010
Company DUNS657731175
Company NameLIGHTMED CORPORATION
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 Batchtrue
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

Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram
Weight20 Kilogram

Device Identifiers

Device Issuing AgencyDevice ID
GS104712826770635 [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 Date2016-09-23

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