GUDIDData
eudamed_udi Primary ID: 58859299130434

ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave (UDI 58859299130434)

Manufactured by Epic International (Thailand) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave - Primary ID 58859299130434

Device Regulatory Overview

The ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave (Model/Catalog Number: 420435) is a medical device manufactured by Epic International (Thailand) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0704 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
420435
Product Code / EMDN
A0704
Device Name
CSTD and Administration Devices
Database Sync Date
2026-08-09 16:28:46

Full Regulatory Attributes

🔒 Token Gated
{
    "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 ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave?

The registered manufacturer of record for ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave is Epic International (Thailand) Co., Ltd..

What is the Primary UDI-DI identifier for ToxiSeal Vial Adaptor (DMA Compatible) for 20 mm Vial Concave?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 58859299130434.

What classification code is assigned to this device?

This device is registered under product classification code A0704.

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