eudamed_udi
Primary ID: 08057143740227
Moonray Precisio (UDI 08057143740227)
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 Precisio - Primary ID 08057143740227
Device Regulatory Overview
The Moonray Precisio (Model/Catalog Number: EMP F2M1 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
- EMP F2M1 V
- Product Code / EMDN
- Z11039017
- Device Name
- Moonray
- Database Sync Date
- 2026-08-09 16:49:12
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 Moonray Precisio?
The registered manufacturer of record for Moonray Precisio is SIMAD S.R.L..
What is the Primary UDI-DI identifier for Moonray Precisio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057143740227.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint