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Guofa Jintan suction catheter (unsterilized) - Taiwan Registration c751c101fb32260e95ca39a8b32faca7

Access comprehensive regulatory information for Guofa Jintan suction catheter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c751c101fb32260e95ca39a8b32faca7 and manufactured by K. F. (JIN TAN) SPECIAL TEXTILES CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS 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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c751c101fb32260e95ca39a8b32faca7
Registration Details
Taiwan FDA Registration: c751c101fb32260e95ca39a8b32faca7
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Device Details

Guofa Jintan suction catheter (unsterilized)
TW: ๅœ‹็™ผ้‡‘ๅฃ‡ๆŠฝๅธๅฐŽ็ฎก(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c751c101fb32260e95ca39a8b32faca7

DHA04600002104

Company Information

Product Details

A device for removing liquids or semi-solids from the patient's upper airway.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

Input;; Chinese goods

Dates and Status

Oct 27, 2005

Oct 27, 2025