gudid
Primary ID: V3
eScreen eReader (UDI V3)
Manufactured by ESCREEN, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for eScreen eReader - Primary ID V3
Device Regulatory Overview
The eScreen eReader (Model/Catalog Number: V3) is a medical device manufactured by ESCREEN, INC.. This product is indexed under FDA Product Code / Category Classification LDJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V3
- Product Code / EMDN
- LDJ
- Device Name
- The eScreen eReader is a sophisticated appliance that uses digital technology to scan the test lid of a sealed eCup, providing an 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 applicant tracking system.
- Database Sync Date
- 2026-08-09 09:49:14
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of eScreen eReader?
The registered manufacturer of record for eScreen eReader is ESCREEN, INC..
What is the Primary UDI-DI identifier for eScreen eReader?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V3.
What classification code is assigned to this device?
This device is registered under product classification code LDJ.
Similar Classification Devices (LDJ)
Other Devices by ESCREEN, INC.
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