Aerolase LightPod Era

GUDID 08631720003020

Medical Aesthetic Laser for skin resurfacing

AEROLASE CORPORATION

Ophthalmic solid-state laser system, photodisruption

• Primary Device ID: 08631720003020
• NIH Device Record Key: 7810ce72-d8ed-4c9b-a12f-34b838250b19
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aerolase
• Version Model Number: ErbiumXL
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08631720003020 [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: 2021-10-19
• Device Publish Date: 2021-10-11

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