gudid
Primary ID: 0909FCC
0909FCC (UDI 0909FCC)
Manufactured by Rayence Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 0909FCC - Primary ID 0909FCC
Device Regulatory Overview
The 0909FCC (Model/Catalog Number: 0909FCC) is a medical device manufactured by Rayence Co., Ltd.. This product is indexed under FDA Product Code / Category Classification JAA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0909FCC
- Product Code / EMDN
- JAA
- Device Name
- X-ray, Fluoroscopic, image-intensified 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 0909FCC?
The registered manufacturer of record for 0909FCC is Rayence Co., Ltd..
What is the Primary UDI-DI identifier for 0909FCC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0909FCC.
What classification code is assigned to this device?
This device is registered under product classification code JAA.
Similar Classification Devices (JAA)
Other Devices by Rayence Co., Ltd.
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