Taiwan FDA registration a1e3064336dce26b6c227b522eae75df

“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 07, 2014 – Jul 07, 2024Expired
Registration details
Analysis ID
a1e3064336dce26b6c227b522eae75df
License Form
Ministry of Health Medical Device Import No. 026394
Customs Code
DHA05602639403
Company information
Manufacturer
Rayence Co., Ltd.
Manufacturer Country
Korea, Republic of
Authorized Representative
VATECH MEDICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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 07, 2014
Expiry Date
Jul 07, 2024
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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 a1e3064336dce26b6c227b522eae75df 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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