GUDIDData
gudid Primary ID: 9009

Double Diffusion Plates (10/pkg) (UDI 9009)

Manufactured by HELENA LABORATORIES CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Double Diffusion Plates (10/pkg) - Primary ID 9009

Device Regulatory Overview

The Double Diffusion Plates (10/pkg) (Model/Catalog Number: 9009) is a medical device manufactured by HELENA LABORATORIES CORPORATION. This product is indexed under FDA Product Code / Category Classification JZR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9009
Product Code / EMDN
JZR
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 Double Diffusion Plates (10/pkg)?

The registered manufacturer of record for Double Diffusion Plates (10/pkg) is HELENA LABORATORIES CORPORATION.

What is the Primary UDI-DI identifier for Double Diffusion Plates (10/pkg)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9009.

What classification code is assigned to this device?

This device is registered under product classification code JZR.

Programmatic Export

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

JSON API Endpoint