DEVICE: 0909FCB (08800018600900)
Device Identifier (DI) Information
0909FCB
0909FCB
In Commercial Distribution
Rayence Co., Ltd.
0909FCB
In Commercial Distribution
Rayence Co., Ltd.
The 0909FCB flat panel detector employs a CsI:Tl scintillator for X-ray-to-light converter. Column-structurized CsI:Tl scintillator have high resolution performance due to much less light blurring, and is thus available for a longer period of time. CMOS active pixel detector makes extremely low noise level and highly sensitive performance. Due to seamless one chip CMOS, there is no data missing or artifacts.
The high physical and functional performance of 0909FCB gives competitive image quality.
The RAW files can be further processed as DICOM compatible image files by separate console SW for a radiographic diagnosis and analysis.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
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61108 | Indirect flat panel x-ray detector |
An electrically-powered, cassette-like device intended to be used as part of an x-ray system to detect x-ray images following exposure, and create a digital signal; it is not dedicated to imaging of a specific anatomy. It includes two types of transducing technology (i.e., indirect): a scintillator [e.g. caesium iodide (CsI)] screen converts x-ray energy into light, followed by the conversion of light into a digital signal by photodiode array. The image data can be sent to an appropriate processing unit through a wired or wireless connection (e.g., Wi-Fi). It may be used in place of a fixed detector in x-ray imaging systems, e.g., as part of a digital imaging conversion system.
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FDA Product Code
[?]Product Code | Product Code Name |
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MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) |
JAA | System, X-Ray, Fluoroscopic, Image-Intensified |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K212753 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Handling Environment Atmospheric Pressure: between 70 and 106 KiloPascal |
Handling Environment Humidity: between 30 and 75 Percent (%) Relative Humidity |
Handling Environment Temperature: between 10 and 35 Degrees Celsius |
Storage Environment Atmospheric Pressure: between 86 and 106 KiloPascal |
Storage Environment Humidity: between 10 and 75 Percent (%) Relative Humidity |
Storage Environment Temperature: between -10 and 60 Degrees Celsius |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
70845d50-ba3c-4f80-b457-639b3a578c73
November 08, 2021
1
October 29, 2021
November 08, 2021
1
October 29, 2021
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
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Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined