GUDIDData
gudid Primary ID: 1484000

AggRAM Analyzer, Windows 2000 (110V/220V) (UDI 1484000)

Manufactured by HELENA LABORATORIES CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AggRAM Analyzer, Windows 2000 (110V/220V) - Primary ID 1484000

Device Regulatory Overview

The AggRAM Analyzer, Windows 2000 (110V/220V) (Model/Catalog Number: 1484000) is a medical device manufactured by HELENA LABORATORIES CORPORATION. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1484000
Product Code / EMDN
JPA
Device Name
Database Sync Date
2026-08-09 09:36:16

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 AggRAM Analyzer, Windows 2000 (110V/220V)?

The registered manufacturer of record for AggRAM Analyzer, Windows 2000 (110V/220V) is HELENA LABORATORIES CORPORATION.

What is the Primary UDI-DI identifier for AggRAM Analyzer, Windows 2000 (110V/220V)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1484000.

What classification code is assigned to this device?

This device is registered under product classification code JPA.

Programmatic Export

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

JSON API Endpoint