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"Nipro" plastic injection needle - Taiwan Registration 886202a13edbfc05a917aadcd7f16d21

Access comprehensive regulatory information for "Nipro" plastic injection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 886202a13edbfc05a917aadcd7f16d21 and manufactured by NIPRO (SHANGHAI) CO., LTD.;; NIPRO CORPORATION. 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 (THAILAND) CORPORATION LIMITED, 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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886202a13edbfc05a917aadcd7f16d21
Registration Details
Taiwan FDA Registration: 886202a13edbfc05a917aadcd7f16d21
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Device Details

"Nipro" plastic injection needle
TW: โ€œๅฐผๆ™ฎๆด›โ€ๅก‘่† ๆณจๅฐ„้‡
Risk Class 2

Registration Details

886202a13edbfc05a917aadcd7f16d21

DHA04200019202

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Input;; Chinese goods

Dates and Status

Jan 20, 2009

Jan 20, 2029

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