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“Rayence” Medical Image Processing Unit - Taiwan Registration 36f872e73565062cd04a527fa3561969

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 36f872e73565062cd04a527fa3561969 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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36f872e73565062cd04a527fa3561969
Registration Details
Taiwan FDA Registration: 36f872e73565062cd04a527fa3561969
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Device Details

“Rayence” Medical Image Processing Unit
TW: “瑞恩斯”醫學影像處理器
Risk Class 2
MD

Registration Details

36f872e73565062cd04a527fa3561969

Ministry of Health Medical Device Import No. 026958

DHA05602695800

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Jan 28, 2015

Jan 28, 2025

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