gudid
Primary ID: AST-804
Capillus (UDI AST-804)
Manufactured by CAPILLUS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capillus - Primary ID AST-804
Device Regulatory Overview
The Capillus (Model/Catalog Number: AST-804) is a medical device manufactured by CAPILLUS, LLC. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AST-804
- Product Code / EMDN
- OLP
- Device Name
- Red and blue light therapy device to reduce the appearance of fine lines and wrinkles and treat mild to moderate acne vulgaris.
- Database Sync Date
- 2026-08-09 09:05:25
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Capillus?
The registered manufacturer of record for Capillus is CAPILLUS, LLC.
What is the Primary UDI-DI identifier for Capillus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AST-804.
What classification code is assigned to this device?
This device is registered under product classification code OLP.
Similar Classification Devices (OLP)
Other Devices by CAPILLUS, LLC
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