gudid Primary ID: E&I V3 - New

eREADER (UDI E&I V3 - New)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The eREADER (Model/Catalog Number: E&I V3 - New) is a medical device manufactured by ESCREEN, INC.. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: E&I V3 - New
Product Code / EMDN: JJQ
Device Name: The eScreen eREADER is a sophisticated appliance that uses digital technology to scan the test lid of a sealed eCup, providingan automated, objective, confidential testing process. The eREADER uses bar code technology, coupled with optical imaging,to electronically capture the drug test results from eCups without the subjectivity of a clinician reading them. Within 15 minutes,the eREADER automatically reports a negative eCUP urine drug screen back to you via your account or another applicanttracking system.
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 eREADER?

The registered manufacturer of record for eREADER is ESCREEN, INC..

What is the Primary UDI-DI identifier for eREADER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E&I V3 - New.

What classification code is assigned to this device?

This device is registered under product classification code JJQ.

Similar Classification Devices (JJQ)

Other Devices by ESCREEN, INC.

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