Taiwan FDA registration 1410e7dc9870fc5aa7009b8f386c6e7a
"Taknik" X-ray system
TW: “塔克尼克”X光系統
Taiwan·Risk Class 2·TECHNIX S. P. A.·Registered Oct 01, 2018 – Oct 01, 2028ActiveRegistration details
- Analysis ID
- 1410e7dc9870fc5aa7009b8f386c6e7a
- Customs Code
- DHAS5603153905
Company information
- Manufacturer
- TECHNIX S. P. A.
- Manufacturer Country
- Italy
- Authorized Representative
- PIEZOMED INTERNATIONAL INC.
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.1720 移動式X光系統;; P.1620 連續或間斷式透視X光機
- 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
- Oct 01, 2018
- Expiry Date
- Oct 01, 2028
About this record
Access comprehensive regulatory information for "Taknik" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1410e7dc9870fc5aa7009b8f386c6e7a and manufactured by TECHNIX S. P. A.. The authorized representative in Taiwan is PIEZOMED INTERNATIONAL INC..
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