eudamed_udi Primary ID: 04719875599019

EpiFaith Syringe (Luer slip) (UDI 04719875599019)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EpiFaith Syringe (Luer slip) (Model/Catalog Number: EF-01SLR, EF-02SNR, EF-01SLL) is a medical device manufactured by Flat Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: EF-01SLR, EF-02SNR, EF-01SLL
Product Code / EMDN: A020101
Device Name: EpiFaith Syringe
Database Sync Date: 2026-08-09 18:59:18

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 EpiFaith Syringe (Luer slip)?

The registered manufacturer of record for EpiFaith Syringe (Luer slip) is Flat Medical Co., Ltd..

What is the Primary UDI-DI identifier for EpiFaith Syringe (Luer slip)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719875599019.

What classification code is assigned to this device?

This device is registered under product classification code A020101.

Similar Classification Devices (A020101)

Other Devices by Flat Medical Co., Ltd.

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