Crono (UDI F)

Manufactured by CANE' SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Crono (Model/Catalog Number: F) is a medical device manufactured by CANE' SPA. This product is indexed under FDA Product Code / Category Classification FRN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: F
Product Code / EMDN: FRN
Device Name: The Crono F is an ambulatory drug delivery pump designed to deliver subcutaneous and intravenous pulsatile infusion.
Database Sync Date: 2026-08-09 09:04:32

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 Crono?

The registered manufacturer of record for Crono is CANE' SPA.

What is the Primary UDI-DI identifier for Crono?

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

What classification code is assigned to this device?

This device is registered under product classification code FRN.

Similar Classification Devices (FRN)

Other Devices by CANE' SPA

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