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"Three forces" single-use venous blood collection needles - Taiwan Registration b12bcb44db6ce98742587d914a2f4414

Access comprehensive regulatory information for "Three forces" single-use venous blood collection needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b12bcb44db6ce98742587d914a2f4414 and manufactured by Liuyang SANLI Medical Technology Development Co., Ltd.. The authorized representative in Taiwan is WE SERVE ENTERPRISE 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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b12bcb44db6ce98742587d914a2f4414
Registration Details
Taiwan FDA Registration: b12bcb44db6ce98742587d914a2f4414
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Device Details

"Three forces" single-use venous blood collection needles
TW: โ€œไธ‰ๅŠ›โ€ ไธ€ๆฌกๆ€งไฝฟ็”จ้œ่„ˆๆŽก่ก€้‡
Risk Class 2

Registration Details

b12bcb44db6ce98742587d914a2f4414

DHA09200092002

Company Information

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Input;; Chinese goods

Dates and Status

Aug 23, 2018

Aug 23, 2023