Taiwan FDA registration 6b11a9a6d5916a9a5dcf4867bc218c19

“Rayence” Medical Image Processing Unit

TW: “瑞恩斯” 醫學影像處理器
Taiwan flagTaiwan·Risk Class 2·MD·Rayence Co., Ltd.·Registered Sep 08, 2023 – Sep 08, 2028Active
Registration details
Analysis ID
6b11a9a6d5916a9a5dcf4867bc218c19
License Form
Ministry of Health Medical Device Import No. 036599
Customs Code
DHA05603659901
Company information
Manufacturer
Rayence Co., Ltd.
Manufacturer Country
Korea, Republic of
Authorized Representative
VATECH MEDICAL CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P1650 fluoroscopic X-ray image intensifier
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 08, 2023
Expiry Date
Sep 08, 2028
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About this record

Access comprehensive regulatory information for “Rayence” Medical Image Processing Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b11a9a6d5916a9a5dcf4867bc218c19 and manufactured by Rayence Co., Ltd.. The authorized representative in Taiwan is VATECH MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Rayence Co., Ltd., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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