Taiwan FDA registration c751c101fb32260e95ca39a8b32faca7

Guofa Jintan suction catheter (unsterilized)

TW: 國發金壇抽吸導管(未滅菌)

Taiwan·Risk Class 1·K. F. (JIN TAN) SPECIAL TEXTILES CO., LTD.·Registered Oct 27, 2005 – Oct 27, 2025Expired

Registration details

Analysis ID: c751c101fb32260e95ca39a8b32faca7
Customs Code: DHA04600002104

Company information

Manufacturer: K. F. (JIN TAN) SPECIAL TEXTILES CO., LTD.
Manufacturer Country: China
Authorized Representative: K.F. MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: A device for removing liquids or semi-solids from the patient's upper airway.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.6810 Pneumatic bronchial suction guide tube
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Oct 27, 2005
Expiry Date: Oct 27, 2025

About this record

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..

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