Taiwan FDA registration 90e915adcf573bc583522c9ae4f9f1ad
"Deerjian" X-ray diagnostic system and its accessories
TW: “迪爾健” X光診斷系統及其配件
Taiwan·Risk Class 2·DRGEM CORPORATION·Registered Feb 19, 2021 – Feb 19, 2026ExpiredRegistration details
- Analysis ID
- 90e915adcf573bc583522c9ae4f9f1ad
- Customs Code
- DHAS5603433300
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
- 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
- Feb 19, 2021
- Expiry Date
- Feb 19, 2026
About this record
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.
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