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"Deerjian" X-ray diagnostic system - Taiwan Registration 4e40033fe623d531c33a232fdcc6ea6f

Access comprehensive regulatory information for "Deerjian" 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 4e40033fe623d531c33a232fdcc6ea6f and manufactured by DRGEM CORPORATION. The authorized representative in Taiwan is NAN KAI CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DRGEM 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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4e40033fe623d531c33a232fdcc6ea6f
Registration Details
Taiwan FDA Registration: 4e40033fe623d531c33a232fdcc6ea6f
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Device Details

"Deerjian" X-ray diagnostic system
TW: โ€œ่ฟช็ˆพๅฅโ€ Xๅ…‰่จบๆ–ท็ณป็ตฑ
Risk Class 2

Registration Details

4e40033fe623d531c33a232fdcc6ea6f

DHAS5602862402

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

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jul 11, 2016

Jul 11, 2026

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