GUDIDData
gudid Primary ID: EBT4 Max-EA Film Insert 3

Gafchromic (UDI EBT4 Max-EA Film Insert 3)

Manufactured by ASHLAND SPECIALTY INGREDIENTS G.P.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gafchromic - Primary ID EBT4 Max-EA Film Insert 3

Device Regulatory Overview

The Gafchromic (Model/Catalog Number: EBT4 Max-EA Film Insert 3) is a medical device manufactured by ASHLAND SPECIALTY INGREDIENTS G.P.. This product is indexed under FDA Product Code / Category Classification IWZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EBT4 Max-EA Film Insert 3
Product Code / EMDN
IWZ
Device Name
Database Sync Date
2026-08-09 09:09:51

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 Gafchromic?

The registered manufacturer of record for Gafchromic is ASHLAND SPECIALTY INGREDIENTS G.P..

What is the Primary UDI-DI identifier for Gafchromic?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EBT4 Max-EA Film Insert 3.

What classification code is assigned to this device?

This device is registered under product classification code IWZ.

Programmatic Export

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

JSON API Endpoint