Aerolase LightPod Era

GUDID 00086317200302

Medical aesthetic laser

AEROLASE CORPORATION

Ophthalmic solid-state laser system, photodisruption

• Primary Device ID: 00086317200302
• NIH Device Record Key: 9a3a5205-e948-4ede-88c3-d7337e65a805
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aerolase
• Version Model Number: Erbium
• Catalog Number: LightPod Era
• Company DUNS: 014927581
• Company Name: AEROLASE CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00086317200302 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2019-12-10
• Device Publish Date: 2019-12-02

On-Brand Devices [Aerolase]

• 00863172000304: Medical aesthetic laser
• 00086317200302: Medical aesthetic laser
• 08631720003020: Medical Aesthetic Laser for skin resurfacing
• 00863172000311: medical aesthetic laser for skin resurfacing