Taiwan FDA registration 07356344c2fb49383f7a9748e287d7e7
"DORNIER" orthopedic seismometer
TW: “多尼爾”骨科震波儀
Taiwan·Risk Class 3·DORNIER MEDTECH SYSTEMS GMBH·Registered Dec 10, 2010 – Dec 10, 2015CancelledRegistration details
- Analysis ID
- 07356344c2fb49383f7a9748e287d7e7
- Customs Code
- DHA00602183209
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)
- N Orthopedics
- Product Type (Level 2)
- N.0001 骨科用體外震波系統
- Import Information
- 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". input
Dates and status
- Registration Date
- Dec 10, 2010
- Expiry Date
- Dec 10, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "DORNIER" orthopedic seismometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 07356344c2fb49383f7a9748e287d7e7 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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