Taiwan FDA registration 46bdd15ecd01b1907f446923a0309314

"Fresenius" Vople Flow artificial kidney

TW: “費森尤斯”沃普流人工腎臟
Taiwan flagTaiwan·Risk Class 2·FRESENIUS MEDICAL CARE NORTH AMERICA·Registered Nov 26, 2009 – Nov 26, 2024Expired
Registration details
Analysis ID
46bdd15ecd01b1907f446923a0309314
Customs Code
DHA00602073009
Company information
Manufacturer Country
United States
Product details
Intended Use
Freseniuswop Flow series artificial kidneys are designed for acute and chronic hemodialysis and are suitable for single and multiple use. When going through the reprocessing process, please follow the method described or recommended in this product manual. Multiple uses by the same patient only.
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
Nov 26, 2009
Expiry Date
Nov 26, 2024
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About this record

Access comprehensive regulatory information for "Fresenius" Vople Flow artificial kidney in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46bdd15ecd01b1907f446923a0309314 and manufactured by FRESENIUS MEDICAL CARE NORTH AMERICA. 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 NORTH AMERICA, 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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