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"Qinda" medical gauze (sterilization) - Taiwan Registration 236df9b2dbd9bce9e940d79b305a95c7

Access comprehensive regulatory information for "Qinda" medical gauze (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 236df9b2dbd9bce9e940d79b305a95c7 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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236df9b2dbd9bce9e940d79b305a95c7
Registration Details
Taiwan FDA Registration: 236df9b2dbd9bce9e940d79b305a95c7
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Device Details

"Qinda" medical gauze (sterilization)
TW: โ€œๅ‹ค้”โ€้†ซ็™‚็”จ็ด—ๅธƒ(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

236df9b2dbd9bce9e940d79b305a95c7

DHA04400616200

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Absorbent Fiber (J.5300)".

J General hospital and personal use equipment

J.5300 ้†ซ็™‚็”จๅธๆ”ถ็บ–็ถญ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Sep 20, 2007

Sep 20, 2022

Apr 12, 2024

Cancellation Information

Logged out

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