gudid
Primary ID: BW090
Cavex Bite&White ABC Masterkit (UDI BW090)
Manufactured by Cavex Holland B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cavex Bite&White ABC Masterkit - Primary ID BW090
Device Regulatory Overview
The Cavex Bite&White ABC Masterkit (Model/Catalog Number: BW090) is a medical device manufactured by Cavex Holland B.V.. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BW090
- Product Code / EMDN
- EEG
- Device Name
- Dental Whitening Agent
- Database Sync Date
- 2026-08-09 09:07:32
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 Cavex Bite&White ABC Masterkit?
The registered manufacturer of record for Cavex Bite&White ABC Masterkit is Cavex Holland B.V..
What is the Primary UDI-DI identifier for Cavex Bite&White ABC Masterkit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BW090.
What classification code is assigned to this device?
This device is registered under product classification code EEG.
Similar Classification Devices (EEG)
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