Lightlas SeLecTor Deux

GUDID 04712826770932

LIGHTMED CORPORATION

General/multiple surgical frequency-doubled solid-state laser system

• Primary Device ID: 04712826770932
• NIH Device Record Key: 87a42bcd-d832-46e2-b113-007124d10bff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lightlas SeLecTor Deux
• Version Model Number: ST0021
• 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 Dimensions

• Weight: 28 Kilogram

Device Identifiers

Device Issuing Agency	Device ID
GS1	04712826770932 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090774

FDA Product Code

• HQF: Laser, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-16
• Device Publish Date: 2020-04-08

On-Brand Devices [Lightlas SeLecTor Deux]

• 04712826770598: SLT0005
• 04712826770581: SLT0001
• 04712826770574: SLT0000
• 04712826770963: ST0024
• 04712826770956: ST0023
• 04712826770949: ST0022
• 04712826770932: ST0021
• 04712826770925: ST0020