eudamed_udi
Primary ID: 08436042241835
Cubeta flúor dobles grandes Royal (UDI 08436042241835)
Manufactured by J RIPOLL SL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cubeta flúor dobles grandes Royal - Primary ID 08436042241835
Device Regulatory Overview
The Cubeta flúor dobles grandes Royal (Model/Catalog Number: FDGR) is a medical device manufactured by J RIPOLL SL. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FDGR
- Product Code / EMDN
- Q010503
- Device Name
- CUBETAS FLUOR /FLUORIDE TRAYS
- Database Sync Date
- 2026-08-09 16:29:56
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 Cubeta flúor dobles grandes Royal?
The registered manufacturer of record for Cubeta flúor dobles grandes Royal is J RIPOLL SL.
What is the Primary UDI-DI identifier for Cubeta flúor dobles grandes Royal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08436042241835.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
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