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Nipro Tripartite Live Plug - Taiwan Registration f3752044e9eec2b71ebc731f53d4f45b

Access comprehensive regulatory information for Nipro Tripartite Live Plug in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3752044e9eec2b71ebc731f53d4f45b 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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f3752044e9eec2b71ebc731f53d4f45b
Registration Details
Taiwan FDA Registration: f3752044e9eec2b71ebc731f53d4f45b
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Device Details

Nipro Tripartite Live Plug
TW: ๅฐผๆ™ฎๆด›ไธ‰ๆ–นๆดปๆ “
Risk Class 2

Registration Details

f3752044e9eec2b71ebc731f53d4f45b

DHA05603741305

Company Information

Product Details

Details are as detailed as approved Chinese instructions

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E.4290 Arterial vascular bypass surgery with contact pistons, multi-pipe connections or attachments

import

Dates and Status

Sep 14, 2024

Sep 14, 2029