gudid
Primary ID: 577275WW
OptraGate Assortment (UDI 577275WW)
Manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OptraGate Assortment - Primary ID 577275WW
Device Regulatory Overview
The OptraGate Assortment (Model/Catalog Number: 577275WW) is a medical device manufactured by IVOCLAR VIVADENT AKTIENGESELLSCHAFT. This product is indexed under FDA Product Code / Category Classification EIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 577275WW
- Product Code / EMDN
- EIF
- Device Name
- OptraGate Assortment
- Database Sync Date
- 2026-08-09 09:01:02
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of OptraGate Assortment?
The registered manufacturer of record for OptraGate Assortment is IVOCLAR VIVADENT AKTIENGESELLSCHAFT.
What is the Primary UDI-DI identifier for OptraGate Assortment?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 577275WW.
What classification code is assigned to this device?
This device is registered under product classification code EIF.
Similar Classification Devices (EIF)
Other Devices by IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint