gudid
Primary ID: 686072AN
IPS Empress Direct (UDI 686072AN)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IPS Empress Direct - Primary ID 686072AN
Device Regulatory Overview
The IPS Empress Direct (Model/Catalog Number: 686072AN) 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
- 686072AN
- Product Code / EMDN
- EBF
- Device Name
- Empress Direct System 6x3g/2x1.8g/Pad
- 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 IPS Empress Direct?
The registered manufacturer of record for IPS Empress Direct is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for IPS Empress Direct?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 686072AN.
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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