Taiwan FDA registration f647407843fdf221e7ffdd1972fcf1fb

"Shimadzu" digital X-ray fluoroscopy system

TW: “島津”數位X光透視攝影系統
Taiwan flagTaiwan·Risk Class 2·Shimane Shimadzu Corporation·Registered Dec 03, 2009 – Dec 03, 2029Active
Registration details
Analysis ID
f647407843fdf221e7ffdd1972fcf1fb
Customs Code
DHAS0602045903
Company information
Manufacturer Country
Japan
Authorized Representative
SAN KANG INSTRUMENTS CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1730 照相透視X光系統
Import Information
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
Registration Date
Dec 03, 2009
Expiry Date
Dec 03, 2029
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About this record

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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