eudamed_udi
Primary ID: 08058302602424
ATLANTE (UDI 08058302602424)
Manufactured by Malvestio Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ATLANTE - Primary ID 08058302602424
Device Regulatory Overview
The ATLANTE (Model/Catalog Number: 378300B) is a medical device manufactured by Malvestio Spa. This product is indexed under FDA Product Code / Category Classification V08060105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 378300B
- Product Code / EMDN
- V08060105
- Device Name
- ATLANTE
- Database Sync Date
- 2026-08-09 16:47:12
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 ATLANTE?
The registered manufacturer of record for ATLANTE is Malvestio Spa.
What is the Primary UDI-DI identifier for ATLANTE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08058302602424.
What classification code is assigned to this device?
This device is registered under product classification code V08060105.
Similar Classification Devices (V08060105)
Other Devices by Malvestio Spa
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint