gudid
Primary ID: 628885AN
IvoBase (UDI 628885AN)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IvoBase - Primary ID 628885AN
Device Regulatory Overview
The IvoBase (Model/Catalog Number: 628885AN) 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
- 628885AN
- Product Code / EMDN
- EBI
- Device Name
- IvoBase Hybrid Polymer, Monomer, Funnels, Wax parts, Ventilation filter, Separating Fluid, Spatula
- Database Sync Date
- 2026-08-09 09:01:05
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 IvoBase?
The registered manufacturer of record for IvoBase is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for IvoBase?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 628885AN.
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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