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"Pademk" Gastroenterology-Urology Bioexamination Equipment (Sterilization) - Taiwan Registration 9731956f8f6e280b75de25d58e268819

Access comprehensive regulatory information for "Pademk" Gastroenterology-Urology Bioexamination Equipment (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9731956f8f6e280b75de25d58e268819 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., 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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9731956f8f6e280b75de25d58e268819
Registration Details
Taiwan FDA Registration: 9731956f8f6e280b75de25d58e268819
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Device Details

"Pademk" Gastroenterology-Urology Bioexamination Equipment (Sterilization)
TW: โ€œๅธ•ๅฐ‡ๅ…‹โ€่…ธ่ƒƒ็ง‘-ๆณŒๅฐฟ็ง‘็”Ÿๆชขๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9731956f8f6e280b75de25d58e268819

DHA04400736809

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Gastroenterology-Urology Bioexamination Devices (H.1075)".

H Gastroenterology and urology

H.1075 ่…ธ่ƒƒ็ง‘-ๆณŒๅฐฟ็ง‘็”Ÿๆชขๅ™จๆขฐ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 06, 2009

Jan 06, 2019

Aug 05, 2022

Cancellation Information

Logged out

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