Taiwan FDA registration c03a7d77a444d0958cb7c69a5bd22d66

"Fresenius" synthetic membrane hemodialyzer - FX series

TW: “費森尤斯”人工合成膜血液透析器-FX系列
Taiwan flagTaiwan·Risk Class 2·FRESENIUS MEDICAL CARE JAPAN K.K. BUZEN PLANT·Registered Feb 27, 2009 – Feb 27, 2029Active
Registration details
Analysis ID
c03a7d77a444d0958cb7c69a5bd22d66
Customs Code
DHA00601968007
Company information
Manufacturer Country
Japan
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.5860 高滲透性之血液透析系統
Import Information
import
Dates and status
Registration Date
Feb 27, 2009
Expiry Date
Feb 27, 2029
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About this record

Access comprehensive regulatory information for "Fresenius" synthetic membrane hemodialyzer - FX series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c03a7d77a444d0958cb7c69a5bd22d66 and manufactured by FRESENIUS MEDICAL CARE JAPAN K.K. BUZEN PLANT. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRESENIUS MEDICAL CARE SMAD, 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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