Taiwan FDA registration e9f352bea2a1017dfa16b7e396afcbfa

"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 Mar 02, 2004 – Mar 02, 2019Cancelled
Registration details
Analysis ID
e9f352bea2a1017dfa16b7e396afcbfa
Customs Code
DHA00601056402
Company information
Manufacturer Country
Japan
Authorized Representative
HUA CHIANG MEDICAL CO., LTD.
Product details
Product Type (Level 1)
H Gastroenterology and urology
Import Information
import
Dates and status
Registration Date
Mar 02, 2004
Expiry Date
Mar 02, 2019
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 e9f352bea2a1017dfa16b7e396afcbfa 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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