eudamed_udi Primary ID: D-COLESTEROLO-LDLKR

COLESTEROLO DIRETTO LDL (UDI D-COLESTEROLO-LDLKR)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The COLESTEROLO DIRETTO LDL (Model/Catalog Number: FCC204-2) is a medical device manufactured by FUTURLAB S.R.L.. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FCC204-2
Product Code / EMDN: W01010221
Device Name: COLESTEROLO DIRETTO LDL
Database Sync Date: 2026-08-09 17:08:19

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 COLESTEROLO DIRETTO LDL?

The registered manufacturer of record for COLESTEROLO DIRETTO LDL is FUTURLAB S.R.L..

What is the Primary UDI-DI identifier for COLESTEROLO DIRETTO LDL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-COLESTEROLO-LDLKR.

What classification code is assigned to this device?

This device is registered under product classification code W01010221.

Similar Classification Devices (W01010221)

Other Devices by FUTURLAB S.R.L.

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