gudid
Primary ID: MD Duo
Capillus (UDI MD 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 MD Duo
Device Regulatory Overview
The Capillus (Model/Catalog Number: MD 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
- MD 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
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 MD 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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint