eudamed_udi Primary ID: 08015013500067

NOVA (UDI 08015013500067)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The NOVA (Model/Catalog Number: 500067) is a medical device manufactured by EUROPROSAN S.P.A.. This product is indexed under FDA Product Code / Category Classification T04010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 500067
Product Code / EMDN: T04010103
Device Name: NOVA
Database Sync Date: 2026-08-09 16:29:19

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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Frequently Asked Questions

Who is the primary manufacturer of NOVA?

The registered manufacturer of record for NOVA is EUROPROSAN S.P.A..

What is the Primary UDI-DI identifier for NOVA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015013500067.

What classification code is assigned to this device?

This device is registered under product classification code T04010103.

Similar Classification Devices (T04010103)

Other Devices by EUROPROSAN S.P.A.

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