Taiwan FDA registration 5e668eef1486e3b69200a47a68eba05d
"Macolon" sterilized sputum suction pack (sterilized)
TW: “瑪科隆” 滅菌抽痰包 (滅菌)
Taiwan·Risk Class 1·ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.·Registered Sep 24, 2012 – Sep 24, 2017CancelledRegistration details
- Analysis ID
- 5e668eef1486e3b69200a47a68eba05d
- Customs Code
- DHA04600175400
Company information
- Manufacturer Country
- China
- Authorized Representative
- Marcolon GmbH
Product details
- Intended Use
- Limited to the first level of identification scope of "Tracheobronchial Suction Catheter (D.6810)" and "Gloves for Patient Examination (J.6250)" under the Measures for the Administration of 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
- Input;; Chinese goods;; QMS/QSD
Dates and status
- Registration Date
- Sep 24, 2012
- Expiry Date
- Sep 24, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Macolon" sterilized sputum suction 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 5e668eef1486e3b69200a47a68eba05d and manufactured by ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Marcolon GmbH.
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