Taiwan FDA registration b12bcb44db6ce98742587d914a2f4414

"Three forces" single-use venous blood collection needles

TW: “三力” 一次性使用靜脈採血針
Taiwan flagTaiwan·Risk Class 2·Liuyang SANLI Medical Technology Development Co., Ltd.·Registered Aug 23, 2018 – Aug 23, 2023Expired
Registration details
Analysis ID
b12bcb44db6ce98742587d914a2f4414
Customs Code
DHA09200092002
Company information
Manufacturer Country
China
Authorized Representative
WE SERVE ENTERPRISE CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5570 Subcutaneous single-chamber needle
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Aug 23, 2018
Expiry Date
Aug 23, 2023
About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices