Taiwan FDA registration 01553b4878db40ba34e5e03c15ac9deb

"Kawasumi" hemodialyzer

TW: 「川澄」 血液透析器
Taiwan flagTaiwan·Risk Class 2·KAWASUMI LABORATORIES INC. MIE FACTORY·Registered Jan 13, 2005 – Jan 13, 2020Cancelled
Registration details
Analysis ID
01553b4878db40ba34e5e03c15ac9deb
Customs Code
DHA00601100800
Company information
Manufacturer Country
Japan
Authorized Representative
EXCELSIOR MEDICAL CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.5820 血液透析系統及其附件
Import Information
import
Dates and status
Registration Date
Jan 13, 2005
Expiry Date
Jan 13, 2020
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Kawasumi" hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01553b4878db40ba34e5e03c15ac9deb and manufactured by KAWASUMI LABORATORIES INC. MIE FACTORY. The authorized representative in Taiwan is EXCELSIOR MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KAWASUMI LABORATORIES,INC. MIE FACTORY, and 1 recent registrations in the same category. 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.

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