PodSKAN HF Diagnostic X-ray System (UDI 303-002665-0)
Manufactured by SKANRAY TECHNOLOGIES LIMITED
Device Regulatory Overview
The PodSKAN HF Diagnostic X-ray System (Model/Catalog Number: 303-002665-0) is a medical device manufactured by SKANRAY TECHNOLOGIES LIMITED. This product is indexed under FDA Product Code / Category Classification KPR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 303-002665-0
- Product Code / EMDN
- KPR
- Device Name
- PodSKAN is an advanced high frequency type X-Ray system designed for superior image quality with powerful 2.8KW generator and very low leakage radiation. The system houses two microprocessors, one for control/supervisory functions and another one man-machine/User interface. It can be easily plugged into 16A Wall socket with 120 VAC or 240 VAC, 50/60 Hz.. The technology incorporates feedback circuits to ensure highest accuracy & reproducibility of X-Ray output.
- Database Sync Date
- 2026-08-09 09:29:39
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 PodSKAN HF Diagnostic X-ray System?
The registered manufacturer of record for PodSKAN HF Diagnostic X-ray System is SKANRAY TECHNOLOGIES LIMITED.
What is the Primary UDI-DI identifier for PodSKAN HF Diagnostic X-ray System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 303-002665-0.
What classification code is assigned to this device?
This device is registered under product classification code KPR.
Similar Classification Devices (KPR)
Other Devices by SKANRAY TECHNOLOGIES LIMITED
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