Taiwan FDA registration 4e40033fe623d531c33a232fdcc6ea6f

"Deerjian" X-ray diagnostic system

TW: “迪爾健” X光診斷系統
Taiwan flagTaiwan·Risk Class 2·DRGEM CORPORATION·Registered Jul 11, 2016 – Jul 11, 2026Expired
Registration details
Analysis ID
4e40033fe623d531c33a232fdcc6ea6f
Customs Code
DHAS5602862402
Company information
Manufacturer
DRGEM CORPORATION
Manufacturer Country
Korea, Republic of
Authorized Representative
NAN KAI CORPORATION
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.1680 固定式X光系統
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Jul 11, 2016
Expiry Date
Jul 11, 2026
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About this record

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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