GUDIDData
gudid Primary ID: CEFALY Connected

Cefaly (UDI CEFALY Connected)

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 CEFALY Connected

Device Regulatory Overview

The Cefaly (Model/Catalog Number: CEFALY Connected) 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
CEFALY Connected
Product Code / EMDN
PCC
Device Name
CEFALY Connected is indicated to be used for:Acute treatment of migraine with or without aura in patients 18 years of age or older.Preventative treatment of migraine in patients 18 years of age or older.
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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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 CEFALY Connected.

What classification code is assigned to this device?

This device is registered under product classification code PCC.

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