Taiwan FDA registration f2f8199bfc6e007a55e7ca05e72a8c34
"Strauss" powered laser guide tube
TW: “史特勞斯”動力雷射導引導管
Taiwan·Risk Class 2·SPECTRANETICS CORPORATION·Registered Oct 22, 2009 – Oct 22, 2014CancelledRegistration details
- Analysis ID
- f2f8199bfc6e007a55e7ca05e72a8c34
- Customs Code
- DHA00602025202
Company information
- Manufacturer
- SPECTRANETICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Oct 22, 2009
- Expiry Date
- Oct 22, 2014
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Strauss" powered laser guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f2f8199bfc6e007a55e7ca05e72a8c34 and manufactured by SPECTRANETICS CORPORATION. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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