Taiwan FDA registration fb447df32c9d2ad3ea09f820f213c71e

"Qinda" sputum suction package (sterilized)

TW: "勤達"抽痰包(滅菌)

Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered May 14, 2018 – May 14, 2023Expired

Registration details

Analysis ID: fb447df32c9d2ad3ea09f820f213c71e
Customs Code: DHA09401904701

Company information

Manufacturer: HOSPITECH MANUFACTURING SERVICES SDN. BHD.
Manufacturer Country: Malaysia
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.6810 Pneumatic bronchial suction guide tube
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: May 14, 2018
Expiry Date: May 14, 2023

About this record

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..

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