eudamed_udi
Primary ID: 08054529351695
NOVOX CUP M 2pcs. (UDI 08054529351695)
Manufactured by MOSS S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOVOX CUP M 2pcs. - Primary ID 08054529351695
Device Regulatory Overview
The NOVOX CUP M 2pcs. (Model/Catalog Number: NCP-M-L2) is a medical device manufactured by MOSS S.p.A.. This product is indexed under FDA Product Code / Category Classification M040413 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NCP-M-L2
- Product Code / EMDN
- M040413
- Device Name
- NOVOX CUP
- Database Sync Date
- 2026-08-09 17:59:18
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 NOVOX CUP M 2pcs.?
The registered manufacturer of record for NOVOX CUP M 2pcs. is MOSS S.p.A..
What is the Primary UDI-DI identifier for NOVOX CUP M 2pcs.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054529351695.
What classification code is assigned to this device?
This device is registered under product classification code M040413.
Similar Classification Devices (M040413)
Other Devices by MOSS S.p.A.
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