LightLas 532/810

GUDID 04712826770673

The 532/810 Laser System is included laser console, laser delivery unit, and ophthalmic powered table. There are 3 boxs individually.

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 ID: 04712826770673
• NIH Device Record Key: bbab9e5b-e9e9-4393-bb24-7287fe9904b7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LightLas 532/810
• Version Model Number: ML0012
• Company DUNS: 657731175
• Company Name: LIGHTMED CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04712826770673 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152688

FDA Product Code

• HQF: Laser, Ophthalmic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

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• 04712826770840 - TruScan Pro: 2021-04-21