gudid
Primary ID: 749568
Resin Teeth / DCL / PE (UDI 749568)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Resin Teeth / DCL / PE - Primary ID 749568
Device Regulatory Overview
The Resin Teeth / DCL / PE (Model/Catalog Number: 749568) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification ELM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 749568
- Product Code / EMDN
- ELM
- Device Name
- SR Orthotyp A-D Set of 8 L N2L C4
- 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 Resin Teeth / DCL / PE?
The registered manufacturer of record for Resin Teeth / DCL / PE is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for Resin Teeth / DCL / PE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 749568.
What classification code is assigned to this device?
This device is registered under product classification code ELM.
Similar Classification Devices (ELM)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
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