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"Qinda" examination gloves (unsterilized) - Taiwan Registration 6e17a262b6ecc3cb2f1f96e34666ffda

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..

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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6e17a262b6ecc3cb2f1f96e34666ffda
Registration Details
Taiwan FDA Registration: 6e17a262b6ecc3cb2f1f96e34666ffda
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Device Details

"Qinda" examination gloves (unsterilized)
TW: โ€œๅ‹ค้”โ€ๆชข่จบๆ‰‹ๅฅ—(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

6e17a262b6ecc3cb2f1f96e34666ffda

DHA04400554100

Company Information

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".

J General hospital and personal use equipment

J.6250 ็—…ๆ‚ฃๆชขๆŸฅ็”จๆ‰‹ๅฅ—

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 18, 2007

Jan 18, 2022

Apr 12, 2024

Cancellation Information

Logged out

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