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"Dajin" X-ray diagnostic system - Taiwan Registration f3655026834a4be5f693e0eec21477f3

Access comprehensive regulatory information for "Dajin" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3655026834a4be5f693e0eec21477f3 and manufactured by DRGEM CORPORATION. The authorized representative in Taiwan is WITTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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f3655026834a4be5f693e0eec21477f3
Registration Details
Taiwan FDA Registration: f3655026834a4be5f693e0eec21477f3
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Device Details

"Dajin" X-ray diagnostic system
TW: โ€œ้”ๅ‹โ€Xๅ…‰่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

f3655026834a4be5f693e0eec21477f3

DHAS0602311308

Company Information

Korea, Republic of

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผ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 19, 2011

Dec 19, 2021

Aug 15, 2023

Cancellation Information

Logged out

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