eudamed_udi
Primary ID: 08058302601656
CUBIK (UDI 08058302601656)
Manufactured by Malvestio Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUBIK - Primary ID 08058302601656
Device Regulatory Overview
The CUBIK (Model/Catalog Number: 334555) is a medical device manufactured by Malvestio Spa. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 334555
- Product Code / EMDN
- Y1803
- Device Name
- CUBIK
- Database Sync Date
- 2026-08-09 16:29:41
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 CUBIK?
The registered manufacturer of record for CUBIK is Malvestio Spa.
What is the Primary UDI-DI identifier for CUBIK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058302601656.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
Other Devices by Malvestio Spa
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint