eudamed_udi Primary ID: 08944000597332

JMI (UDI 08944000597332)

Manufactured by JMI SYRINGES & MEDICAL DEVICES LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The JMI (Model/Catalog Number: FP6254) is a medical device manufactured by JMI SYRINGES & MEDICAL DEVICES LTD.. This product is indexed under FDA Product Code / Category Classification C010180 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FP6254
Product Code / EMDN: C010180
Device Name: FP6254: Sterile, Single Use, IV Cannula, 24G (Ø0.70mm x 19mm) with Extra Injection Plug, with Injection Port Luer Lock, Flow Rate: 20 ml/min
Database Sync Date: 2026-08-09 16:29:24

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 JMI?

The registered manufacturer of record for JMI is JMI SYRINGES & MEDICAL DEVICES LTD..

What is the Primary UDI-DI identifier for JMI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08944000597332.

What classification code is assigned to this device?

This device is registered under product classification code C010180.

Similar Classification Devices (C010180)

Other Devices by JMI SYRINGES & MEDICAL DEVICES LTD.

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