Taiwan FDA registration 6e17a262b6ecc3cb2f1f96e34666ffda

"Qinda" examination gloves (unsterilized)

TW: “勤達”檢診手套(未滅菌)

Taiwan·Risk Class 1·HOSPITECH MANUFACTURING SERVICES SDN. BHD.·Registered Jan 18, 2007 – Jan 18, 2022Cancelled

Registration details

Analysis ID: 6e17a262b6ecc3cb2f1f96e34666ffda
Customs Code: DHA04400554100

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 of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6250 病患檢查用手套
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jan 18, 2007
Expiry Date: Jan 18, 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 "Qinda" examination gloves (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6e17a262b6ecc3cb2f1f96e34666ffda and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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