Taiwan FDA registration 121151b1a2295e2a890a018490a109e1

"Fresenius" synthetic membrane hemodialyzer

TW: "費森尤斯"人工合成膜血液透析器
Taiwan flagTaiwan·Risk Class 2·FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH ST. WENDEL PLANT·Registered Oct 16, 2001 – Oct 16, 2026Active
Registration details
Analysis ID
121151b1a2295e2a890a018490a109e1
Customs Code
DHA00600975009
Company information
Manufacturer Country
Germany
Product details
Product Type (Level 1)
H000 胃腸病科學及泌尿科學
Import Information
import
Dates and status
Registration Date
Oct 16, 2001
Expiry Date
Oct 16, 2026
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About this record

Access comprehensive regulatory information for "Fresenius" synthetic membrane hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 121151b1a2295e2a890a018490a109e1 and manufactured by FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH ST. WENDEL PLANT. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH, FRESENIUS MEDICAL CARE SMAD, and 3 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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