GUDIDData
gudid Primary ID: 12019558

InteliQ (UDI 12019558)

Manufactured by BIO-RAD LABORATORIES, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for InteliQ - Primary ID 12019558

Device Regulatory Overview

The InteliQ (Model/Catalog Number: 12019558) is a medical device manufactured by BIO-RAD LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification JJY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
12019558
Product Code / EMDN
JJY
Device Name
InteliQ Specialty Immunoassay Plus Control Level Low MiniPak (A human serum assayed immunoassay control.)
Database Sync Date
2026-08-09 09:23:28

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of InteliQ?

The registered manufacturer of record for InteliQ is BIO-RAD LABORATORIES, INC..

What is the Primary UDI-DI identifier for InteliQ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12019558.

What classification code is assigned to this device?

This device is registered under product classification code JJY.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint