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"Lepu" Anxing single-use angiography catheter - Taiwan Registration 21b8d7f9d24bcc98b7468253e739e75d

Access comprehensive regulatory information for "Lepu" Anxing single-use angiography catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21b8d7f9d24bcc98b7468253e739e75d and manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC 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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21b8d7f9d24bcc98b7468253e739e75d
Registration Details
Taiwan FDA Registration: 21b8d7f9d24bcc98b7468253e739e75d
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Device Details

"Lepu" Anxing single-use angiography catheter
TW: โ€œๆจ‚ๆ™ฎโ€ๅฎ‰่•Žๆ˜Ÿไธ€ๆฌกๆ€งไฝฟ็”จ่ก€็ฎก้€ ๅฝฑๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

21b8d7f9d24bcc98b7468253e739e75d

DHA09200065901

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1200 ่จบๆ–ท็”จ่ก€็ฎกๅ…งๅฐŽ็ฎก

Chinese goods;; input

Dates and Status

Jun 17, 2015

Jun 17, 2020

Jun 16, 2022

Cancellation Information

Logged out

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