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"Xinfeng" tracheobronchial suction catheter (sterilized) - Taiwan Registration 021c41b9b705fe782409d09d2b790b55

Access comprehensive regulatory information for "Xinfeng" tracheobronchial suction catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 021c41b9b705fe782409d09d2b790b55 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. 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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021c41b9b705fe782409d09d2b790b55
Registration Details
Taiwan FDA Registration: 021c41b9b705fe782409d09d2b790b55
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Device Details

"Xinfeng" tracheobronchial suction catheter (sterilized)
TW: โ€œๆ–ฐ่ฑโ€ๆฐฃ็ฎกๆ”ฏๆฐฃ็ฎกๆŠฝๅธๅฐŽ็ฎก(ๆป…่Œ)
Risk Class 1

Registration Details

021c41b9b705fe782409d09d2b790b55

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Feb 22, 2008

Feb 22, 2028