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"Nidris" suction tube with sputum collection box (sterilization) - Taiwan Registration 23eb2ee46d1d8b0decf83c78f67fde66

Access comprehensive regulatory information for "Nidris" suction tube with sputum collection box (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23eb2ee46d1d8b0decf83c78f67fde66 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.

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23eb2ee46d1d8b0decf83c78f67fde66
Registration Details
Taiwan FDA Registration: 23eb2ee46d1d8b0decf83c78f67fde66
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Device Details

"Nidris" suction tube with sputum collection box (sterilization)
TW: "ๅฐผๅพ—็ซ‹ๆ–ฏ" ๆŠฝ็—ฐ็ฎก้™„็—ฐๆถฒๆ”ถ้›†็›’ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

23eb2ee46d1d8b0decf83c78f67fde66

DHA09600317207

Company Information

Product Details

Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

Chinese goods;; Input;; QMS/QSD

Dates and Status

Aug 14, 2017

Aug 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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