gudid
Primary ID: 771206
XPLEX Base (UDI 771206)
Manufactured by Candulor AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XPLEX Base - Primary ID 771206
Device Regulatory Overview
The XPLEX Base (Model/Catalog Number: 771206) is a medical device manufactured by Candulor AG. This product is indexed under FDA Product Code / Category Classification EBI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 771206
- Product Code / EMDN
- EBI
- Device Name
- XPLEX Base F8 98.5-30MM
- Database Sync Date
- 2026-08-09 09:00:28
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 XPLEX Base?
The registered manufacturer of record for XPLEX Base is Candulor AG.
What is the Primary UDI-DI identifier for XPLEX Base?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 771206.
What classification code is assigned to this device?
This device is registered under product classification code EBI.
Similar Classification Devices (EBI)
Other Devices by Candulor AG
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