Taiwan FDA registration 03ac4747eded33799e9c6c6fe411a8e3

"Xinfeng" central venous catheter

TW: "新豐" 中央靜脈導管
Taiwan flagTaiwan·Risk Class 2·SYMPHON MEDICAL TECHNOLOGY CO., LTD.·Registered Oct 23, 2002 – Oct 23, 2027Active
Registration details
Analysis ID
03ac4747eded33799e9c6c6fe411a8e3
Customs Code
DHA00500097404
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
SYMPHON MEDICAL TECHNOLOGY CO., LTD.
Product details
Intended Use
Vacuum.
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1250 Percutaneous catheters
Import Information
Domestic
Dates and status
Registration Date
Oct 23, 2002
Expiry Date
Oct 23, 2027
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About this record

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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