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"Huaxin" sputum suction package (sterilized) - Taiwan Registration f1c48eee93886f8f7875c05647e9e69e

Access comprehensive regulatory information for "Huaxin" 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 f1c48eee93886f8f7875c05647e9e69e and manufactured by ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is MODERN HEALTHCARE CORP..

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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f1c48eee93886f8f7875c05647e9e69e
Registration Details
Taiwan FDA Registration: f1c48eee93886f8f7875c05647e9e69e
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Device Details

"Huaxin" sputum suction package (sterilized)
TW: โ€œ่ฏๆ–ฐโ€ๆŠฝ็—ฐๅŒ… (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f1c48eee93886f8f7875c05647e9e69e

DHA04600146200

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

QMS/QSD;; Chinese goods;; input

Dates and Status

Sep 09, 2011

Sep 09, 2021

Aug 23, 2023

Cancellation Information

Logged out

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