Taiwan FDA registration d56c39a86f1de5f959bd548a73c80e3e
Asahi Haoji series digital full-mouth/head X-ray equipment
TW: 朝日豪品機系列數位全口/頭顱X光設備
Taiwan·Risk Class 2·ASAHIROENTGEN IND. CO., LTD.·Registered Sep 15, 2017 – Sep 15, 2027ActiveRegistration details
- Analysis ID
- d56c39a86f1de5f959bd548a73c80e3e
- Customs Code
- DHAS5603023009
Company information
- Manufacturer
- ASAHIROENTGEN IND. CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- TOP GEAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.1800 口腔外X光照射系統
- 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
- Sep 15, 2017
- Expiry Date
- Sep 15, 2027
About this record
Access comprehensive regulatory information for Asahi Haoji series digital full-mouth/head X-ray equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d56c39a86f1de5f959bd548a73c80e3e and manufactured by ASAHIROENTGEN IND. CO., LTD.. The authorized representative in Taiwan is TOP GEAL CO., LTD..
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