Taiwan FDA registration 9051c235ce6e83e2a5e659f3778edff6

"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 Sep 05, 2008 – Sep 05, 2023Expired
Registration details
Analysis ID
9051c235ce6e83e2a5e659f3778edff6
Customs Code
DHA00601920302
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
Sep 05, 2008
Expiry Date
Sep 05, 2023
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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 9051c235ce6e83e2a5e659f3778edff6 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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