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"Qinda" sputum suction package (sterilized) - Taiwan Registration fb447df32c9d2ad3ea09f820f213c71e

Access comprehensive regulatory information for "Qinda" sputum suction package (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fb447df32c9d2ad3ea09f820f213c71e and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT 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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fb447df32c9d2ad3ea09f820f213c71e
Registration Details
Taiwan FDA Registration: fb447df32c9d2ad3ea09f820f213c71e
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Device Details

"Qinda" sputum suction package (sterilized)
TW: "ๅ‹ค้”"ๆŠฝ็—ฐๅŒ…(ๆป…่Œ)
Risk Class 1

Registration Details

fb447df32c9d2ad3ea09f820f213c71e

DHA09401904701

Company Information

Product Details

Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

Input;; QMS/QSD

Dates and Status

May 14, 2018

May 14, 2023