gudid
Primary ID: 740234WW
Variolink Esthetic (UDI 740234WW)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Variolink Esthetic - Primary ID 740234WW
Device Regulatory Overview
The Variolink Esthetic (Model/Catalog Number: 740234WW) 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
- 740234WW
- Product Code / EMDN
- EBF
- Device Name
- cements
- 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 Variolink Esthetic?
The registered manufacturer of record for Variolink Esthetic is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Variolink Esthetic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 740234WW.
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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