gudid
Primary ID: 701184AL
Cervitec Plus (UDI 701184AL)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cervitec Plus - Primary ID 701184AL
Device Regulatory Overview
The Cervitec Plus (Model/Catalog Number: 701184AL) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification LBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 701184AL
- Product Code / EMDN
- LBH
- Device Name
- Cervitec Plus Test Pack 3x0.25g
- 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 Cervitec Plus?
The registered manufacturer of record for Cervitec Plus is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Cervitec Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 701184AL.
What classification code is assigned to this device?
This device is registered under product classification code LBH.
Similar Classification Devices (LBH)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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