gudid
Primary ID: 686310
Telio CAD (UDI 686310)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Telio CAD - Primary ID 686310
Device Regulatory Overview
The Telio CAD (Model/Catalog Number: 686310) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification EBG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 686310
- Product Code / EMDN
- EBG
- Device Name
- Telio CAD LT A1 98.5-25mm/1
- Database Sync Date
- 2026-08-09 09:01:03
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 Telio CAD?
The registered manufacturer of record for Telio CAD is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Telio CAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 686310.
What classification code is assigned to this device?
This device is registered under product classification code EBG.
Similar Classification Devices (EBG)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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