Taiwan FDA registration efa6b8da2f6dfb115f73dcdd902bd10b
“Kawasumi Laboratories” Hollow Fiber Dialyzer
TW: “川澄化工”人工腎臟
Taiwan·Risk Class 2·MD·KAWASUMI LABORATORIES,INC. MIE FACTORY·Registered Nov 25, 2014 – Nov 25, 2019CancelledRegistration details
- Analysis ID
- efa6b8da2f6dfb115f73dcdd902bd10b
- License Form
- Ministry of Health Medical Device Import No. 026794
- Customs Code
- DHA05602679406
Company information
- Manufacturer
- KAWASUMI LABORATORIES,INC. MIE FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5820 Hemodialysis systems and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 25, 2014
- Expiry Date
- Nov 25, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Kawasumi Laboratories” Hollow Fiber Dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number efa6b8da2f6dfb115f73dcdd902bd10b and manufactured by KAWASUMI LABORATORIES,INC. MIE FACTORY. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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