gudid Primary ID: SH1FSELUX

SH1FSELUX (UDI SH1FSELUX)

Manufactured by AGILENT TECHNOLOGIES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SH1FSELUX (Model/Catalog Number: SH1FSELUX) is a medical device manufactured by AGILENT TECHNOLOGIES, INC.. This product is indexed under FDA Product Code / Category Classification JJQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SH1FSELUX
Product Code / EMDN: JJQ
Device Name: Multi-Mode Microplate Reader
Database Sync Date: 2026-08-09 09:57:21

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 SH1FSELUX?

The registered manufacturer of record for SH1FSELUX is AGILENT TECHNOLOGIES, INC..

What is the Primary UDI-DI identifier for SH1FSELUX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SH1FSELUX.

What classification code is assigned to this device?

This device is registered under product classification code JJQ.

Similar Classification Devices (JJQ)

Other Devices by AGILENT TECHNOLOGIES, INC.

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