Taiwan FDA registration 500c5375cea2a3beb75f24566a550f02
"Kawasumi" membrane plasma separator
TW: "川澄" 膜型血漿分離器
Registration details
- Analysis ID
- 500c5375cea2a3beb75f24566a550f02
- Customs Code
- DHA00601082106
Company information
- Manufacturer
- KAWASUMI LABORATORIES,INC. MIE FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- MUTUAL TRADING CO., LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Aug 27, 2004
- Expiry Date
- Aug 27, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kawasumi" membrane plasma separator in Taiwan's medical device market through Pure Global AI's free database. is registered under number 500c5375cea2a3beb75f24566a550f02 and manufactured by KAWASUMI LABORATORIES,INC. MIE FACTORY. The authorized representative in Taiwan is MUTUAL TRADING 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