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"Shimadzu" digital X-ray fluoroscopy system - Taiwan Registration f647407843fdf221e7ffdd1972fcf1fb

Access comprehensive regulatory information for "Shimadzu" digital X-ray fluoroscopy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f647407843fdf221e7ffdd1972fcf1fb and manufactured by Shimane Shimadzu Corporation. The authorized representative in Taiwan is SAN KANG INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Shimadzu Corporation;; Shimane Shimadzu Corporation, and 1 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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f647407843fdf221e7ffdd1972fcf1fb
Registration Details
Taiwan FDA Registration: f647407843fdf221e7ffdd1972fcf1fb
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Device Details

"Shimadzu" digital X-ray fluoroscopy system
TW: โ€œๅณถๆดฅโ€ๆ•ธไฝXๅ…‰้€่ฆ–ๆ”ๅฝฑ็ณป็ตฑ
Risk Class 2

Registration Details

f647407843fdf221e7ffdd1972fcf1fb

DHAS0602045903

Company Information

Product Details

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

P Radiology Science

P.1730 ็…ง็›ธ้€่ฆ–Xๅ…‰็ณป็ตฑ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Dec 03, 2009

Dec 03, 2029

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