gudid
Primary ID: VI011
Cavex Vibringe (UDI VI011)
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 Vibringe - Primary ID VI011
Device Regulatory Overview
The Cavex Vibringe (Model/Catalog Number: VI011) is a medical device manufactured by Cavex Holland B.V.. This product is indexed under FDA Product Code / Category Classification EIC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VI011
- Product Code / EMDN
- EIC
- Device Name
- Edodontic Irrigating Device
- 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 Vibringe?
The registered manufacturer of record for Cavex Vibringe is Cavex Holland B.V..
What is the Primary UDI-DI identifier for Cavex Vibringe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VI011.
What classification code is assigned to this device?
This device is registered under product classification code EIC.
Similar Classification Devices (EIC)
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