Taiwan FDA registration 2c13af8d60ab11cb5ded4334318ecf0f
"Andmei" magnetic wave pulse therapy machine
TW: “安德美”磁波脈衝治療機
Taiwan·Risk Class 2·Ondamed GmbH·Registered Sep 16, 2013 – Sep 16, 2018CancelledRegistration details
- Analysis ID
- 2c13af8d60ab11cb5ded4334318ecf0f
- Customs Code
- DHA05602541700
Company information
- Manufacturer
- Ondamed GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- JI CHANG ENTERPRISE CO.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- import
Dates and status
- Registration Date
- Sep 16, 2013
- Expiry Date
- Sep 16, 2018
- Cancellation Date
- Jun 17, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自行鍵入
About this record
Access comprehensive regulatory information for "Andmei" magnetic wave pulse therapy machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2c13af8d60ab11cb5ded4334318ecf0f and manufactured by Ondamed GmbH. The authorized representative in Taiwan is JI CHANG ENTERPRISE CO..
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