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"Meidiken sodium" suction regulator (unsterilized) - Taiwan Registration 138c245f09b204ab18cccd57734d7417

Access comprehensive regulatory information for "Meidiken sodium" 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 138c245f09b204ab18cccd57734d7417 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is YI LIN ENTERPRISE 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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138c245f09b204ab18cccd57734d7417
Registration Details
Taiwan FDA Registration: 138c245f09b204ab18cccd57734d7417
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Device Details

"Meidiken sodium" suction regulator (unsterilized)
TW: โ€œๆข…ๅปธ่‚ฏ้ˆ‰โ€ๅธๅผ•่ชฟ็ฏ€ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

138c245f09b204ab18cccd57734d7417

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

Aug 05, 2013

Aug 05, 2018

Jun 16, 2022

Cancellation Information

Logged out

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