Taiwan FDA registration 53cffc5e5c7e8880b6a6c658d8f5b43f

"Kinda" sputum pack (sterile)

TW: "勤達" 抽痰包 (無菌)

Taiwan·Risk Class 1·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered Aug 12, 2008 – Aug 12, 2018Cancelled

Registration details

Analysis ID: 53cffc5e5c7e8880b6a6c658d8f5b43f
Customs Code: DHA04600056100

Company information

Manufacturer: BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Tracheobronchial Suction Catheter (D.6810) and Gloves for Patient Examination (J.6250)".
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: Input;; QMS/QSD;; Chinese goods

Dates and status

Registration Date: Aug 12, 2008
Expiry Date: Aug 12, 2018
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Kinda" sputum pack (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 53cffc5e5c7e8880b6a6c658d8f5b43f and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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