gudid
Primary ID: 742012
Ivotion Base (UDI 742012)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ivotion Base - Primary ID 742012
Device Regulatory Overview
The Ivotion Base (Model/Catalog Number: 742012) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification EBI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 742012
- Product Code / EMDN
- EBI
- Device Name
- Ivotion Denture Material Kit A2/Pink-V
- Database Sync Date
- 2026-08-09 09:01:03
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 Ivotion Base?
The registered manufacturer of record for Ivotion Base is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Ivotion Base?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 742012.
What classification code is assigned to this device?
This device is registered under product classification code EBI.
Similar Classification Devices (EBI)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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