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"Kenmax" Vacuum Powered Body Fluid Absorption Device (Sterilization) - Taiwan Registration 8e5ac967156da1d8189a847d0560709f

Access comprehensive regulatory information for "Kenmax" Vacuum Powered Body Fluid Absorption Device (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8e5ac967156da1d8189a847d0560709f and manufactured by KENDALL KENMEX, A DIVISION OF, TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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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8e5ac967156da1d8189a847d0560709f
Registration Details
Taiwan FDA Registration: 8e5ac967156da1d8189a847d0560709f
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Device Details

"Kenmax" Vacuum Powered Body Fluid Absorption Device (Sterilization)
TW: โ€œ่‚ฏ้บฅๅธโ€ ็œŸ็ฉบๅ‹•ๅŠ›ๅผ้ซ”ๆถฒๅธๆ”ถๅ™จๅ…ท (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8e5ac967156da1d8189a847d0560709f

DHA04401113909

Company Information

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".

J General hospital and personal use equipment

J.6740 Vacuum-powered fluid absorption apparatus

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Dec 05, 2011

Dec 05, 2016

Mar 16, 2017

Cancellation Information

Logged out

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