Taiwan FDA registration 00a8fe662d791427ad7229a602b369ed
"Pademk" neurostimulator
TW: “帕將克”神經刺激器
Taiwan·Risk Class 2·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered Oct 05, 2012 – Oct 05, 2017CancelledRegistration details
- Analysis ID
- 00a8fe662d791427ad7229a602b369ed
- Customs Code
- DHA00602398301
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.2775 Electronic peripheral nerve stimulator
- Import Information
- import
Dates and status
- Registration Date
- Oct 05, 2012
- Expiry Date
- Oct 05, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pademk" neurostimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 00a8fe662d791427ad7229a602b369ed and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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