eudamed_udi
Primary ID: 08800070202050
ZENEX PLUS Fixture (UDI 08800070202050)
Manufactured by Izenimplant Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZENEX PLUS Fixture - Primary ID 08800070202050
Device Regulatory Overview
The ZENEX PLUS Fixture (Model/Catalog Number: ZPSR4020) is a medical device manufactured by Izenimplant Co.,Ltd. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZPSR4020
- Product Code / EMDN
- P01020101
- Device Name
- ZENEX PLUS Fixture
- Database Sync Date
- 2026-08-09 16:28:44
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 ZENEX PLUS Fixture?
The registered manufacturer of record for ZENEX PLUS Fixture is Izenimplant Co.,Ltd.
What is the Primary UDI-DI identifier for ZENEX PLUS Fixture?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800070202050.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
Other Devices by Izenimplant Co.,Ltd
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