Taiwan FDA registration fbb5e1badce19dc67b3bc63961a20cbc
Venous embolization clears the catheter
TW: 靜脈栓塞清除導管
Taiwan·CLINICAL PLASTIC PRODUCTS S.A.·Registered Feb 15, 1993 – Feb 15, 1998CancelledRegistration details
- Analysis ID
- fbb5e1badce19dc67b3bc63961a20cbc
- Customs Code
- DHA00600684709
Company information
- Manufacturer
- CLINICAL PLASTIC PRODUCTS S.A.
- Manufacturer Country
- Switzerland
- Authorized Representative
- MAX-ALLIED CO., LTD.
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Feb 15, 1993
- Expiry Date
- Feb 15, 1998
- Cancellation Date
- Aug 23, 1999
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Venous embolization clears the catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number fbb5e1badce19dc67b3bc63961a20cbc and manufactured by CLINICAL PLASTIC PRODUCTS S.A.. The authorized representative in Taiwan is MAX-ALLIED 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