gudid
Primary ID: 706585US
Tetric Prime (UDI 706585US)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tetric Prime - Primary ID 706585US
Device Regulatory Overview
The Tetric Prime (Model/Catalog Number: 706585US) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 706585US
- Product Code / EMDN
- EBF
- Device Name
- Tetric Prime Refill 20x0.25g A3
- Database Sync Date
- 2026-08-09 09:01:02
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 Tetric Prime?
The registered manufacturer of record for Tetric Prime is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Tetric Prime?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 706585US.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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