Taiwan FDA registration 4dc143ac20e03d0d87c27f334f3af812

"Nidris" single-use sputum suction kit (sterilization)

TW: "尼得立斯" 一次性使用吸痰包 (滅菌)

Taiwan·Risk Class 1·ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.·Registered Sep 26, 2017 – Sep 26, 2022Cancelled

Registration details

Analysis ID: 4dc143ac20e03d0d87c27f334f3af812
Customs Code: DHA09600322604

Company information

Manufacturer: ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: NEEDLELESS CORPORATION

Product details

Intended Use: 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.
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 26, 2017
Expiry Date: Sep 26, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

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.