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"Deerjian" X-ray diagnostic system and its accessories - Taiwan Registration 90e915adcf573bc583522c9ae4f9f1ad

Access comprehensive regulatory information for "Deerjian" X-ray diagnostic system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90e915adcf573bc583522c9ae4f9f1ad and manufactured by DRGEM CORPORATION. The authorized representative in Taiwan is NAN KAI CORPORATION.

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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90e915adcf573bc583522c9ae4f9f1ad
Registration Details
Taiwan FDA Registration: 90e915adcf573bc583522c9ae4f9f1ad
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Device Details

"Deerjian" X-ray diagnostic system and its accessories
TW: โ€œ่ฟช็ˆพๅฅโ€ Xๅ…‰่จบๆ–ท็ณป็ตฑๅŠๅ…ถ้…ไปถ
Risk Class 2

Registration Details

90e915adcf573bc583522c9ae4f9f1ad

DHAS5603433300

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

Feb 19, 2021

Feb 19, 2026