Taiwan FDA registration 8826ec81d7de1230a41ea957bb3ba3d2

"Xinfeng" Tracheobronchial Suction Catheter Pack (Sterilized)

TW: “新豐” 氣管支氣管抽吸導管包 (滅菌)

Taiwan·Risk Class 1·SYMPHON MEDICAL TECHNOLOGY CO., LTD.·Registered Feb 19, 2014 – Feb 19, 2029Active

Registration details

Analysis ID: 8826ec81d7de1230a41ea957bb3ba3d2

Company information

Manufacturer: SYMPHON MEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SYMPHON MEDICAL TECHNOLOGY CO., LTD.

Product details

Intended Use: It is limited to the first level of identification of the "Tracheobronchial Suction Catheter (D.6810)" and "Gloves for Patient Examination (J.6250)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment;; D Anesthesiology Science
Product Type (Level 2): J.6250 Gloves for patient examination;; D.6810 Tracheobronchial suction tubes
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Feb 19, 2014
Expiry Date: Feb 19, 2029

About this record

Access comprehensive regulatory information for "Xinfeng" Tracheobronchial Suction Catheter Pack (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8826ec81d7de1230a41ea957bb3ba3d2 and manufactured by SYMPHON MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SYMPHON MEDICAL TECHNOLOGY CO., LTD..

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