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"Kinda" sputum pack (sterile) - Taiwan Registration 53cffc5e5c7e8880b6a6c658d8f5b43f

Access comprehensive regulatory information for "Kinda" sputum pack (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 53cffc5e5c7e8880b6a6c658d8f5b43f and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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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53cffc5e5c7e8880b6a6c658d8f5b43f
Registration Details
Taiwan FDA Registration: 53cffc5e5c7e8880b6a6c658d8f5b43f
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Device Details

"Kinda" sputum pack (sterile)
TW: "ๅ‹ค้”" ๆŠฝ็—ฐๅŒ… (็„ก่Œ)
Risk Class 1
Cancelled

Registration Details

53cffc5e5c7e8880b6a6c658d8f5b43f

DHA04600056100

Company Information

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Tracheobronchial Suction Catheter (D.6810) and Gloves for Patient Examination (J.6250)".

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

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

Input;; QMS/QSD;; Chinese goods

Dates and Status

Aug 12, 2008

Aug 12, 2018

Jun 16, 2022

Cancellation Information

Logged out

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