gudid
Primary ID: 04755
dx retainer 1000g (UDI 04755)
Manufactured by DETAX GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for dx retainer 1000g - Primary ID 04755
Device Regulatory Overview
The dx retainer 1000g (Model/Catalog Number: 04755) 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
- 04755
- Product Code / EMDN
- DYJ
- Device Name
- Database Sync Date
- 2026-08-09 09:23:51
Full Regulatory Attributes
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{
"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 dx retainer 1000g?
The registered manufacturer of record for dx retainer 1000g is DETAX GmbH.
What is the Primary UDI-DI identifier for dx retainer 1000g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04755.
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
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