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"Macolon" sterilized sputum suction pack (sterilized) - Taiwan Registration 5e668eef1486e3b69200a47a68eba05d

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.

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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5e668eef1486e3b69200a47a68eba05d
Registration Details
Taiwan FDA Registration: 5e668eef1486e3b69200a47a68eba05d
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Device Details

"Macolon" sterilized sputum suction pack (sterilized)
TW: โ€œ็‘ช็ง‘้š†โ€ ๆป…่ŒๆŠฝ็—ฐๅŒ… (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5e668eef1486e3b69200a47a68eba05d

DHA04600175400

Company Information

Product Details

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.

J General hospital and personal use equipment;; D Anesthesiology Science

J.6250 Gloves for patient examination;; D.6810 Tracheobronchial suction tubes

Input;; Chinese goods;; QMS/QSD

Dates and Status

Sep 24, 2012

Sep 24, 2017

Dec 20, 2019

Cancellation Information

Logged out

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