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"E-Kai" suction regulator (unsterilized) - Taiwan Registration 8e2c0b2a7f3559e11a66220d297b3e5e

Access comprehensive regulatory information for "E-Kai" suction regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8e2c0b2a7f3559e11a66220d297b3e5e and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. 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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8e2c0b2a7f3559e11a66220d297b3e5e
Registration Details
Taiwan FDA Registration: 8e2c0b2a7f3559e11a66220d297b3e5e
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Device Details

"E-Kai" suction regulator (unsterilized)
TW: "ไพๆ„ท"ๅธๅผ•่ชฟ็ฏ€ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8e2c0b2a7f3559e11a66220d297b3e5e

Company Information

Taiwan, Province of China

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

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Dates and Status

Jul 05, 2012

Jul 05, 2017

Sep 19, 2016

Cancellation Information

Logged out

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