E-LIGHT LINE LED MASK H/BLUE

GUDID 08056389700415

ESPANSIONE MARKETING SPA

Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system

• Primary Device ID: 08056389700415
• NIH Device Record Key: c173e793-b31a-40e6-9f74-78dbf6ed32b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E-LIGHT LINE
• Version Model Number: LED MASK H/BLUE
• Catalog Number: LED MASK H/BLUE
• Company DUNS: 339474539
• Company Name: ESPANSIONE MARKETING SPA
• 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: false
• Serial Number: true
• Manufacturing Date: false
• 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	08056389700415 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092734

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: 2020-12-25
• Device Publish Date: 2020-12-17

On-Brand Devices [E-LIGHT LINE]

• 08056389700217: LED MASK/BLUE-05
• 08056389700422: LED MASK H/YELLOW
• 08056389700415: LED MASK H/BLUE
• 08056389700453: LED MASK H-20/BLUE
• 08056389700446: LED MASK H-05/BLUE
• 08056389700712: LAMP570AC
• 08056389701412: LED MASK H-05/YELLOW
• 08056389701375: MASK LM YELLOW/CE-0500
• 08056389701368: MASK LM BLUE/CE-0500
• 08056389701351: MASK LM RED/CE-0500