gudid
Primary ID: 04754
dx retainer 5 kg (UDI 04754)
Manufactured by DETAX GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for dx retainer 5 kg - Primary ID 04754
Device Regulatory Overview
The dx retainer 5 kg (Model/Catalog Number: 04754) is a medical device manufactured by DETAX GmbH. This product is indexed under FDA Product Code / Category Classification DYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04754
- Product Code / EMDN
- DYJ
- Device Name
- Database Sync Date
- 2026-08-09 09:23:51
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 dx retainer 5 kg?
The registered manufacturer of record for dx retainer 5 kg is DETAX GmbH.
What is the Primary UDI-DI identifier for dx retainer 5 kg?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04754.
What classification code is assigned to this device?
This device is registered under product classification code DYJ.
Similar Classification Devices (DYJ)
Other Devices by DETAX GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint