gudid
Primary ID: 754798WW
Adhese Universal (UDI 754798WW)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Adhese Universal - Primary ID 754798WW
Device Regulatory Overview
The Adhese Universal (Model/Catalog Number: 754798WW) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification KLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 754798WW
- Product Code / EMDN
- KLE
- Device Name
- Adhese Univ. Kit VivaPen 1x2ml/100
- 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 Adhese Universal?
The registered manufacturer of record for Adhese Universal is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Adhese Universal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 754798WW.
What classification code is assigned to this device?
This device is registered under product classification code KLE.
Similar Classification Devices (KLE)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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