gudid
Primary ID: 692421WW
TETRIC POWERFILL (UDI 692421WW)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TETRIC POWERFILL - Primary ID 692421WW
Device Regulatory Overview
The TETRIC POWERFILL (Model/Catalog Number: 692421WW) 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
- 692421WW
- Product Code / EMDN
- EBF
- Device Name
- Tetric PowerFill System Kit mixed
- 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 POWERFILL?
The registered manufacturer of record for TETRIC POWERFILL is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for TETRIC POWERFILL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 692421WW.
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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