eudamed_udi
Primary ID: 08057143740494
Moonray Dual (UDI 08057143740494)
Manufactured by SIMAD S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Moonray Dual - Primary ID 08057143740494
Device Regulatory Overview
The Moonray Dual (Model/Catalog Number: EMD F3M1 V) is a medical device manufactured by SIMAD S.R.L.. This product is indexed under FDA Product Code / Category Classification Z11039017 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EMD F3M1 V
- Product Code / EMDN
- Z11039017
- Device Name
- Moonray
- Database Sync Date
- 2026-08-09 16:49:49
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 Moonray Dual?
The registered manufacturer of record for Moonray Dual is SIMAD S.R.L..
What is the Primary UDI-DI identifier for Moonray Dual?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057143740494.
What classification code is assigned to this device?
This device is registered under product classification code Z11039017.
Similar Classification Devices (Z11039017)
Other Devices by SIMAD S.R.L.
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