FDA UDI In Commercial Distribution 🇺🇸 United States

Zerigo Handheld System

DI: 00865522000422 · Model: HD-02 · Zerigo Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Zerigo Handheld System
Primary DI
00865522000422
Version / Model
HD-02
Catalog Number
HD-02-1
Company Name
Zerigo Health, Inc.
Labeler DUNS
079513819
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-06
Public Version
2
Public Version Date
2026-04-03
Public Version Status
Update
Public Device Record Key
d6d7627a-658a-4d85-9492-3402c7e7f8ec

Device Description

Patient access use to the Zerigo Home Light Therapy System, including the provision of the light-emitting device, for the treatment of chronic dermatological conditions such as Psoriasis, Vitiligo, and Eczema for a limited utilization period.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FTC Light, Ultraviolet, Dermatological

GMDN Terms

Code Name
35149 Ultraviolet phototherapy unit, professional

Identifiers

Type ID
Primary 00865522000422
Previous 00865522000415

Premarket Submissions

Submission Number Supplement Number
K170489 000