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"Xinfeng" central venous catheter - Taiwan Registration 03ac4747eded33799e9c6c6fe411a8e3

Access comprehensive regulatory information for "Xinfeng" central venous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03ac4747eded33799e9c6c6fe411a8e3 and manufactured by SYMPHON MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SYMPHON MEDICAL TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Xinfeng Chemical Co., Ltd, SYMPHON MEDICAL TECHNOLOGY CO., LTD., and 2 recent registrations in the same category. 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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03ac4747eded33799e9c6c6fe411a8e3
Registration Details
Taiwan FDA Registration: 03ac4747eded33799e9c6c6fe411a8e3
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Device Details

"Xinfeng" central venous catheter
TW: "ๆ–ฐ่ฑ" ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก
Risk Class 2

Registration Details

03ac4747eded33799e9c6c6fe411a8e3

DHA00500097404

Company Information

Taiwan, Province of China

Product Details

Vacuum.

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

Domestic

Dates and Status

Oct 23, 2002

Oct 23, 2027

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