gudid
Primary ID: 21mm D6
DIA-X FILE (UDI 21mm D6)
Manufactured by DiaDent Group International
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIA-X FILE - Primary ID 21mm D6
Device Regulatory Overview
The DIA-X FILE (Model/Catalog Number: 21mm D6) is a medical device manufactured by DiaDent Group International. This product is indexed under FDA Product Code / Category Classification EKS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21mm D6
- Product Code / EMDN
- EKS
- Device Name
- Dia-X File is a file used for root canal treatment in dentistry.
- Database Sync Date
- 2026-08-09 09:11:05
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DIA-X FILE?
The registered manufacturer of record for DIA-X FILE is DiaDent Group International.
What is the Primary UDI-DI identifier for DIA-X FILE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21mm D6.
What classification code is assigned to this device?
This device is registered under product classification code EKS.
Similar Classification Devices (EKS)
Other Devices by DiaDent Group International
Programmatic Export
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JSON API Endpoint