Taiwan FDA registration bb7bdbaf7a6e2e0ac71e388cf1893b7f
"DORNIER" urological imaging system
TW: “多尼爾”泌尿科影像系統
Taiwan·Risk Class 2·DORNIER MEDTECH SYSTEMS GMBH·Registered Oct 31, 2014 – Oct 31, 2019CancelledRegistration details
- Analysis ID
- bb7bdbaf7a6e2e0ac71e388cf1893b7f
- Customs Code
- DHAS5602666605
Company information
- Manufacturer
- DORNIER MEDTECH SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN 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.1730 照相透視X光系統
- Import Information
- Input;; The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". 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
- Oct 31, 2014
- Expiry Date
- Oct 31, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "DORNIER" urological imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb7bdbaf7a6e2e0ac71e388cf1893b7f and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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