gudid
Primary ID: 1012WCA
1012WCA (UDI 1012WCA)
Manufactured by Rayence Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 1012WCA - Primary ID 1012WCA
Device Regulatory Overview
The 1012WCA (Model/Catalog Number: 1012WCA) is a medical device manufactured by Rayence Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MQB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1012WCA
- Product Code / EMDN
- MQB
- Device Name
- 1012WCA is a digital X-ray flat panel detector that can acquire radiographic images of human anatomy when used with existing radiographic x-ray systems.
- 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 1012WCA?
The registered manufacturer of record for 1012WCA is Rayence Co., Ltd..
What is the Primary UDI-DI identifier for 1012WCA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1012WCA.
What classification code is assigned to this device?
This device is registered under product classification code MQB.
Similar Classification Devices (MQB)
Other Devices by Rayence Co., Ltd.
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