gudid Primary ID: ES-1

EndosacTM (UDI ES-1)

Manufactured by APEX MEDICAL TECHNOLOGIES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EndosacTM (Model/Catalog Number: ES-1) is a medical device manufactured by APEX MEDICAL TECHNOLOGIES, INC.. This product is indexed under FDA Product Code / Category Classification LIO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ES-1
Product Code / EMDN: LIO
Device Name: Specimen Collection Container
Database Sync Date: 2026-08-09 09:49:15

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 EndosacTM?

The registered manufacturer of record for EndosacTM is APEX MEDICAL TECHNOLOGIES, INC..

What is the Primary UDI-DI identifier for EndosacTM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ES-1.

What classification code is assigned to this device?

This device is registered under product classification code LIO.

Similar Classification Devices (LIO)

Other Devices by APEX MEDICAL TECHNOLOGIES, INC.

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