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"Pioneer" intravascular catheter fixation device (sterilization) - Taiwan Registration 82b670010ed22aeddf2c54e774588a71

Access comprehensive regulatory information for "Pioneer" intravascular catheter fixation device (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 82b670010ed22aeddf2c54e774588a71 and manufactured by ZEFON INTERNATIONAL. The authorized representative in Taiwan is CHINA HOSMED INTERNATIONAL INC..

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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82b670010ed22aeddf2c54e774588a71
Registration Details
Taiwan FDA Registration: 82b670010ed22aeddf2c54e774588a71
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Device Details

"Pioneer" intravascular catheter fixation device (sterilization)
TW: โ€œๅ…ˆ้‹’โ€่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

82b670010ed22aeddf2c54e774588a71

DHA04400618305

Company Information

United States

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J.5210 ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

Sep 27, 2007

Sep 27, 2017

Dec 20, 2019

Cancellation Information

Logged out

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