Taiwan FDA registration 68824d946b2265504b42d057bfe541e2
“Spectranetics” Quick-Cross Capture Guidewire Retriever
TW: “史特勞斯”區克斯開普斯導線回收器
Taiwan·Risk Class 2·MD·SPECTRANETICS CORPORATION·Registered Aug 28, 2014 – Aug 28, 2019CancelledRegistration details
- Analysis ID
- 68824d946b2265504b42d057bfe541e2
- License Form
- Ministry of Health Medical Device Import No. 026452
- Customs Code
- DHA05602645204
Company information
- Manufacturer
- SPECTRANETICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 28, 2014
- Expiry Date
- Aug 28, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Spectranetics” Quick-Cross Capture Guidewire Retriever in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68824d946b2265504b42d057bfe541e2 and manufactured by SPECTRANETICS CORPORATION. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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