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"Lily" disposable sterile central venous catheter group - Taiwan Registration ddcfe236a010cf021586bc7e6a2b7e60

Access comprehensive regulatory information for "Lily" disposable sterile central venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddcfe236a010cf021586bc7e6a2b7e60 and manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HURRAYBIO 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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ddcfe236a010cf021586bc7e6a2b7e60
Registration Details
Taiwan FDA Registration: ddcfe236a010cf021586bc7e6a2b7e60
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Device Details

"Lily" disposable sterile central venous catheter group
TW: โ€œ็™พๅˆโ€ไธ€ๆฌกๆ€ง็„ก่Œไธญๅฟƒ้œ่„ˆๅฐŽ็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

ddcfe236a010cf021586bc7e6a2b7e60

DHA09200064200

Company Information

Product Details

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

J General hospital and personal use equipment

J.5200 Endovascular catheters

Input;; Chinese goods

Dates and Status

Jan 06, 2015

Jan 06, 2020

May 19, 2022

Cancellation Information

Logged out

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