gudid
Primary ID: 2430TCA
2430TCA (UDI 2430TCA)
Manufactured by Rayence Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 2430TCA - Primary ID 2430TCA
Device Regulatory Overview
The 2430TCA (Model/Catalog Number: 2430TCA) is a medical device manufactured by Rayence Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MUE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2430TCA
- Product Code / EMDN
- MUE
- Device Name
- Full-Field Digital Mammography System
- Database Sync Date
- 2026-08-09 09:28:55
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 2430TCA?
The registered manufacturer of record for 2430TCA is Rayence Co., Ltd..
What is the Primary UDI-DI identifier for 2430TCA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2430TCA.
What classification code is assigned to this device?
This device is registered under product classification code MUE.
Similar Classification Devices (MUE)
Other Devices by Rayence Co., Ltd.
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