Taiwan FDA registration 88c404353950e20b120605eccb96751f
Meidite guide sheath group
TW: 玫締特導引鞘組
Taiwan·Risk Class 2·TOGO MEDIKIT CO., LTD. HYUGA FACTORY·Registered Jun 21, 2006 – Jun 21, 2016CancelledRegistration details
- Analysis ID
- 88c404353950e20b120605eccb96751f
- Customs Code
- DHA00601672208
Company information
- Manufacturer
- TOGO MEDIKIT CO., LTD. HYUGA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- HSIN TUNG MEDICAL 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
- Import Information
- import
Dates and status
- Registration Date
- Jun 21, 2006
- Expiry Date
- Jun 21, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Meidite guide sheath group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 88c404353950e20b120605eccb96751f and manufactured by TOGO MEDIKIT CO., LTD. HYUGA FACTORY. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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