gudid
Primary ID: Rx Duo
Capillus (UDI Rx Duo)
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 Rx Duo
Device Regulatory Overview
The Capillus (Model/Catalog Number: Rx Duo) is a medical device manufactured by CAPILLUS, LLC. This product is indexed under FDA Product Code / Category Classification OAP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Rx Duo
- Product Code / EMDN
- OAP
- Device Name
- Device for hair growth promotion through photobiomodulation
- Database Sync Date
- 2026-08-09 09:10:02
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 Rx Duo.
What classification code is assigned to this device?
This device is registered under product classification code OAP.
Similar Classification Devices (OAP)
Other Devices by CAPILLUS, LLC
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