gudid
Primary ID: RX DC
myray (UDI RX DC)
Manufactured by CEFLA SOCIETA' COOPERATIVA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for myray - Primary ID RX DC
Device Regulatory Overview
The myray (Model/Catalog Number: RX DC) is a medical device manufactured by CEFLA SOCIETA' COOPERATIVA. This product is indexed under FDA Product Code / Category Classification EHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RX DC
- Product Code / EMDN
- EHD
- Device Name
- MYRAY RX DC - REF: MRPU174WS
- Database Sync Date
- 2026-08-09 09:04:34
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 myray?
The registered manufacturer of record for myray is CEFLA SOCIETA' COOPERATIVA.
What is the Primary UDI-DI identifier for myray?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RX DC.
What classification code is assigned to this device?
This device is registered under product classification code EHD.
Similar Classification Devices (EHD)
Other Devices by CEFLA SOCIETA' COOPERATIVA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint