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"Anqi" one-handed moxibustion needle - Taiwan Registration b8f8ee0b462fac45e9ee04a12c6a187c

Access comprehensive regulatory information for "Anqi" one-handed 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 b8f8ee0b462fac45e9ee04a12c6a187c and manufactured by YU Kuang Industrial CO., LTD.. The authorized representative in Taiwan is AN CHI ACUPUNCTURE 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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b8f8ee0b462fac45e9ee04a12c6a187c
Registration Details
Taiwan FDA Registration: b8f8ee0b462fac45e9ee04a12c6a187c
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Device Details

"Anqi" one-handed moxibustion needle
TW: โ€ๅฎ‰ๆ——โ€ๅ–ฎๆ‰‹้ผ็ธ้‡
Risk Class 2

Registration Details

b8f8ee0b462fac45e9ee04a12c6a187c

DHY00500049407

Company Information

Taiwan, Province of China

Product Details

2301 Therapeutic acupuncture needles

Domestic

Dates and Status

Nov 01, 1991

Feb 09, 2024