eudamed_udi
Primary ID: 08057143740845
Moonray 500 (UDI 08057143740845)
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 500 - Primary ID 08057143740845
Device Regulatory Overview
The Moonray 500 (Model/Catalog Number: EMS F3H2 P) 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
- EMS F3H2 P
- Product Code / EMDN
- Z11039017
- Device Name
- Moonray
- Database Sync Date
- 2026-08-09 16:45:54
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 500?
The registered manufacturer of record for Moonray 500 is SIMAD S.R.L..
What is the Primary UDI-DI identifier for Moonray 500?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057143740845.
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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