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"Synthetic" Fujitec controllable guide sheath - Taiwan Registration 8b58e929a1c4413a31e2714403b8a7fb

Access comprehensive regulatory information for "Synthetic" Fujitec controllable guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b58e929a1c4413a31e2714403b8a7fb and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL 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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8b58e929a1c4413a31e2714403b8a7fb
Registration Details
Taiwan FDA Registration: 8b58e929a1c4413a31e2714403b8a7fb
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Device Details

"Synthetic" Fujitec controllable guide sheath
TW: โ€œๅ…ˆๅฅโ€ๅฏŒๅฃซ้”ๅฏๆŽงๅผๅฐŽๅผ•้ž˜
Risk Class 2
Cancelled

Registration Details

8b58e929a1c4413a31e2714403b8a7fb

DHA04200040503

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Input;; Chinese goods

Dates and Status

Nov 17, 2011

Nov 17, 2016

Aug 14, 2018

Cancellation Information

Logged out

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