eudamed_udi Primary ID: 08904399100025

Healflon Plus (UDI 08904399100025)

Manufactured by Harsoria Healthcare Pvt. Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Healflon Plus (Model/Catalog Number: 0002) is a medical device manufactured by Harsoria Healthcare Pvt. Ltd.. This product is indexed under FDA Product Code / Category Classification C0101010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0002
Product Code / EMDN: C0101010101
Device Name: Intravenous catheter/IV Catheter/IV Cannula
Database Sync Date: 2026-08-09 16:28:45

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 Healflon Plus?

The registered manufacturer of record for Healflon Plus is Harsoria Healthcare Pvt. Ltd..

What is the Primary UDI-DI identifier for Healflon Plus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904399100025.

What classification code is assigned to this device?

This device is registered under product classification code C0101010101.

Similar Classification Devices (C0101010101)

Other Devices by Harsoria Healthcare Pvt. Ltd.

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