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“JSM” Insertion Kit - Taiwan Registration 865973f5218fffe82e2b2e4ef3a2b176

Access comprehensive regulatory information for “JSM” Insertion Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 865973f5218fffe82e2b2e4ef3a2b176 and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.

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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865973f5218fffe82e2b2e4ef3a2b176
Registration Details
Taiwan FDA Registration: 865973f5218fffe82e2b2e4ef3a2b176
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Device Details

“JSM” Insertion Kit
TW: “吉生”穿刺套組
Risk Class 2
MD

Registration Details

865973f5218fffe82e2b2e4ef3a2b176

Ministry of Health Medical Device Manufacturing No. 004631

Company Information

Taiwan, Province of China

Product Details

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

E Cardiovascular devices

E1340 Catheter Guide

Produced in Taiwan, China

Dates and Status

Jun 26, 2014

Jun 26, 2024