gudid
Primary ID: Prevent
Cefaly (UDI Prevent)
Manufactured by Cefaly Technology SPRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cefaly - Primary ID Prevent
Device Regulatory Overview
The Cefaly (Model/Catalog Number: Prevent) is a medical device manufactured by Cefaly Technology SPRL. This product is indexed under FDA Product Code / Category Classification PCC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Prevent
- Product Code / EMDN
- PCC
- Device Name
- The Cefaly Prevent device is indicated for the prophylactic treatment of episodic migraine in adults.
- Database Sync Date
- 2026-08-09 09:57:22
Full Regulatory Attributes
🔒 Token Gated
{
"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 Cefaly?
The registered manufacturer of record for Cefaly is Cefaly Technology SPRL.
What is the Primary UDI-DI identifier for Cefaly?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Prevent.
What classification code is assigned to this device?
This device is registered under product classification code PCC.
Similar Classification Devices (PCC)
Other Devices by Cefaly Technology SPRL
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