Taiwan FDA registration 162fe01e34ccafdf0e49c39e538656b1

"Qinda" sputum collector (sterilized)

TW: "勤達"痰液收集器(滅菌)

Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Oct 25, 2011 – Oct 25, 2021Cancelled

Registration details

Analysis ID: 162fe01e34ccafdf0e49c39e538656b1
Customs Code: DHA04401097501

Company information

Manufacturer: HOSPITECH MANUFACTURING SERVICES SDN BHD
Manufacturer Country: Malaysia
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Oct 25, 2011
Expiry Date: Oct 25, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Qinda" sputum collector (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 162fe01e34ccafdf0e49c39e538656b1 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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