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Timera subcutaneous single-chamber needle (sterilized) - Taiwan Registration e11f2cc93aa433dc6ab40061b1cd352d

Access comprehensive regulatory information for Timera subcutaneous single-chamber needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e11f2cc93aa433dc6ab40061b1cd352d and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY 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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e11f2cc93aa433dc6ab40061b1cd352d
Registration Details
Taiwan FDA Registration: e11f2cc93aa433dc6ab40061b1cd352d
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Device Details

Timera subcutaneous single-chamber needle (sterilized)
TW: ๆ็พŽๆ‹‰็šฎไธ‹ๅ–ฎ่…”้‡๏ผˆๆป…่Œ๏ผ‰
Risk Class 2

Registration Details

e11f2cc93aa433dc6ab40061b1cd352d

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Domestic;; Contract manufacturing

Dates and Status

Sep 29, 2023

Sep 29, 2028