Taiwan FDA registration 0d96c622ac928b2d4bc85b4e9c5528af

"Fresenius" and the membrane flow artificial kidney

TW: “費森尤斯”和膜流人工腎臟

Taiwan·Risk Class 2·FRESENIUS MEDICAL CARE NORTH AMERICA·Registered Nov 26, 2009 – Nov 26, 2024Expired

Registration details

Analysis ID: 0d96c622ac928b2d4bc85b4e9c5528af
Customs Code: DHA00602072901

Company information

Manufacturer: FRESENIUS MEDICAL CARE NORTH AMERICA
Manufacturer Country: United States
Authorized Representative: FRESENIUS MEDICAL CARE TAIWAN CO., LTD.

Product details

Intended Use: Fresenius and Membrane 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

About this record

Access comprehensive regulatory information for "Fresenius" and the membrane 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 0d96c622ac928b2d4bc85b4e9c5528af 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. 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.