Taiwan FDA registration ba89dc51ed7e14450aa1b2c45d38e236
"Graceful" bulbous vasodilated duct
TW: “優美”球中球血管擴張導管
Taiwan·Risk Class 2·NUMED INC.·Registered Jun 08, 2009 – Jun 08, 2019CancelledRegistration details
- Analysis ID
- ba89dc51ed7e14450aa1b2c45d38e236
- Customs Code
- DHA00601989400
Company information
- Manufacturer
- NUMED INC.
- Manufacturer Country
- United States
- Authorized Representative
- SILVER BELL ENTERPRISE 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
- Jun 08, 2009
- Expiry Date
- Jun 08, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Graceful" bulbous vasodilated duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba89dc51ed7e14450aa1b2c45d38e236 and manufactured by NUMED INC.. The authorized representative in Taiwan is SILVER BELL ENTERPRISE INC..
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