Taiwan FDA registration 871c92ae43b8b35e133c1b6c66e20e41

“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 Jul 23, 2013 – Jul 23, 2018Cancelled
Registration details
Analysis ID
871c92ae43b8b35e133c1b6c66e20e41
License Form
Ministry of Health Medical Device Import No. 025209
Customs Code
DHA05602520903
Company information
Manufacturer
Rayence Co., Ltd.
Manufacturer Country
Korea, Republic of
Authorized Representative
VATECH MEDICAL CO., LTD.
Product details
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1650 fluoroscopic X-ray image intensifier
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 23, 2013
Expiry Date
Jul 23, 2018
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 871c92ae43b8b35e133c1b6c66e20e41 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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