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"Nipro" intravenous indwelling needle - Taiwan Registration 4e23ac507b24863da108fb5d13b5f3b2

Access comprehensive regulatory information for "Nipro" intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e23ac507b24863da108fb5d13b5f3b2 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. 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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4e23ac507b24863da108fb5d13b5f3b2
Registration Details
Taiwan FDA Registration: 4e23ac507b24863da108fb5d13b5f3b2
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Device Details

"Nipro" intravenous indwelling needle
TW: โ€œๅฐผๆ™ฎๆด›โ€้œ่„ˆ็•™็ฝฎ้‡
Risk Class 2

Registration Details

4e23ac507b24863da108fb5d13b5f3b2

DHA00601969303

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

import

Dates and Status

Mar 06, 2009

Mar 06, 2029