Taiwan FDA registration 000d315a3663229fbe238c5619df4bcd

"Nipro" hollow fiber dialysis cylinder

TW: “尼普洛”中空纖維透析筒
Taiwan flagTaiwan·Risk Class 2·NIPRO CORPORATION ODATE FACTORY·Registered May 30, 2012 – May 30, 2027Active
Registration details
Analysis ID
000d315a3663229fbe238c5619df4bcd
Customs Code
DHA00602359801
Company information
Manufacturer Country
Japan
Authorized Representative
HUA CHIANG MEDICAL CO., LTD.
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.5820 血液透析系統及其附件
Import Information
import
Dates and status
Registration Date
May 30, 2012
Expiry Date
May 30, 2027
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About this record

Access comprehensive regulatory information for "Nipro" hollow fiber dialysis cylinder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 000d315a3663229fbe238c5619df4bcd 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, 2 companies making similar products including Nipro Corporation Odate Factory, NIPRO CORPORATION ODATE FACTORY, 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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