Zerigo Handheld System HD-02

GUDID 00865522000415

The Zerigo Home Light Therapy System treats chronic dermatological diseases such as Psoriasis, Vitiligo and Eczema.

Zerigo Health, Inc.

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• Primary Device ID: 00865522000415
• NIH Device Record Key: 9813027f-b052-4a90-8d85-568374aceeb5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zerigo Handheld System
• Version Model Number: HD-02
• Catalog Number: HD-02
• Company DUNS: 079513819
• Company Name: Zerigo Health, Inc.
• 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	00865522000415 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170489

FDA Product Code

• FTC: Light, Ultraviolet, Dermatological

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: 2023-03-22
• Device Publish Date: 2023-03-14