gudid
Primary ID: 699995WW
Tetric 100 Universal (UDI 699995WW)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tetric 100 Universal - Primary ID 699995WW
Device Regulatory Overview
The Tetric 100 Universal (Model/Catalog Number: 699995WW) 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
- 699995WW
- Product Code / EMDN
- EBF
- Device Name
- Tetric 100 Univ. Ref. 20x0.25g A1
- 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 100 Universal?
The registered manufacturer of record for Tetric 100 Universal is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Tetric 100 Universal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 699995WW.
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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