Taiwan FDA registration 17ff5175c3c179a83214be12884a6b0a
"Silka" Thopras low-frequency therapy device
TW: “思爾卡”透普拉低頻治療器
Taiwan·Risk Class 2·CELCOM, INC.·Registered Jan 18, 2008 – Jan 18, 2013CancelledRegistration details
- Analysis ID
- 17ff5175c3c179a83214be12884a6b0a
- Customs Code
- DHA00601855002
Company information
- Manufacturer
- CELCOM, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- GOOD LINE INCORPORATION
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
- Jan 18, 2008
- Expiry Date
- Jan 18, 2013
- Cancellation Date
- Jun 03, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Silka" Thopras low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17ff5175c3c179a83214be12884a6b0a and manufactured by CELCOM, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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