"Nidris" single-use sputum suction kit (sterilization) - Taiwan Registration 4dc143ac20e03d0d87c27f334f3af812
Access comprehensive regulatory information for "Nidris" single-use sputum suction kit (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4dc143ac20e03d0d87c27f334f3af812 and manufactured by ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is NEEDLELESS CORPORATION.
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.
Device Details
Product Details
Limited to the first level of identification range of "Tracheobronchial Suction Catheter (D.6810)" and "Gloves for Patient Examination (J.6250)" under the Measures for the Administration of Medical Equipment.
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 26, 2017
Sep 26, 2022
Apr 12, 2024
Cancellation Information
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