gudid Primary ID: DPC-114

iScreen (UDI DPC-114)

Manufactured by Instant Technologies, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The iScreen (Model/Catalog Number: DPC-114) is a medical device manufactured by Instant Technologies, Inc.. This product is indexed under FDA Product Code / Category Classification LCM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DPC-114
Product Code / EMDN: LCM
Device Name: iScreen PCP Panel(Urine) 25T
Database Sync Date: 2026-08-09 09:31:19

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 iScreen?

The registered manufacturer of record for iScreen is Instant Technologies, Inc..

What is the Primary UDI-DI identifier for iScreen?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DPC-114.

What classification code is assigned to this device?

This device is registered under product classification code LCM.

Similar Classification Devices (LCM)

Other Devices by Instant Technologies, Inc.

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