Taiwan FDA registration e670fb3a33782aa2ed58574f1ae1c87d
"Melod" pyrok thrombus removal catheter
TW: “美樂得”派若克血栓清除導管
Taiwan·Risk Class 2·MEDRAD INC.·Registered Jun 01, 2007 – Jun 01, 2017CancelledRegistration details
- Analysis ID
- e670fb3a33782aa2ed58574f1ae1c87d
- Customs Code
- DHA00601811000
Company information
- Manufacturer
- MEDRAD INC.
- Manufacturer Country
- United States
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Jun 01, 2007
- Expiry Date
- Jun 01, 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 "Melod" pyrok thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e670fb3a33782aa2ed58574f1ae1c87d and manufactured by MEDRAD INC.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices