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"Xinli" single-use Y-connector kit - Taiwan Registration 4dda184f73f887604a5c5d4a51fb3614

Access comprehensive regulatory information for "Xinli" single-use Y-connector kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dda184f73f887604a5c5d4a51fb3614 and manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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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4dda184f73f887604a5c5d4a51fb3614
Registration Details
Taiwan FDA Registration: 4dda184f73f887604a5c5d4a51fb3614
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Device Details

"Xinli" single-use Y-connector kit
TW: โ€œๆ˜•ๅŠ›โ€ไธ€ๆฌกๆ€งไฝฟ็”จYๅž‹้€ฃๆŽฅๅ™จๅฅ—ไปถ
Risk Class 2

Registration Details

4dda184f73f887604a5c5d4a51fb3614

DHA09200097702

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.4290 Arterial vascular bypass surgery with contact pistons, multi-pipe connections or attachments

Input;; Chinese goods

Dates and Status

Jan 18, 2019

Jan 18, 2029