Taiwan FDA registration b53abe137ba7f66d0513769d1c7c18b2

"Nipro" dialysis tube for dialysis

TW: "尼普洛" 洗腎用透析筒
Taiwan flagTaiwan·Risk Class 2·Nipro Corporation Odate Factory·Registered May 02, 1990 – Feb 09, 2029Active
Registration details
Analysis ID
b53abe137ba7f66d0513769d1c7c18b2
Customs Code
DHA00600588502
Company information
Manufacturer Country
Japan
Authorized Representative
HUA CHIANG MEDICAL CO., LTD.
Product details
Product Type (Level 1)
0333 Dialysis tube (artificial kidney)
Import Information
import
Dates and status
Registration Date
May 02, 1990
Expiry Date
Feb 09, 2029
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About this record

Access comprehensive regulatory information for "Nipro" dialysis tube for dialysis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b53abe137ba7f66d0513769d1c7c18b2 and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Nipro Corporation Odate 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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