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Tenri needle moxibustion needle - Taiwan Registration 24c91ca06ffc72e61d4865b52e0fefa7

Access comprehensive regulatory information for Tenri needle moxibustion needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24c91ca06ffc72e61d4865b52e0fefa7 and manufactured by Jiangsu Tianxie Medical Instrument Co.,Ltd.. The authorized representative in Taiwan is GREEN HOPE CORPORATION.

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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24c91ca06ffc72e61d4865b52e0fefa7
Registration Details
Taiwan FDA Registration: 24c91ca06ffc72e61d4865b52e0fefa7
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Device Details

Tenri needle moxibustion needle
TW: ๅคฉๅˆฉ้‡็ธ้‡
Risk Class 2

Registration Details

24c91ca06ffc72e61d4865b52e0fefa7

DHA09200100103

Company Information

Product Details

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

J General hospital and personal use equipment

J.5580 Needle moxibustion needle

Input;; Chinese goods

Dates and Status

Mar 06, 2019

Mar 06, 2029