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“Headstar” Handhold Suction Unit (Non-sterile) - Taiwan Registration 2b06a74b3ee351bcb1c218baddb2b826

Access comprehensive regulatory information for “Headstar” Handhold Suction Unit (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b06a74b3ee351bcb1c218baddb2b826 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is HEADSTAR MEDICAL PRODUCTS 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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2b06a74b3ee351bcb1c218baddb2b826
Registration Details
Taiwan FDA Registration: 2b06a74b3ee351bcb1c218baddb2b826
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Device Details

“Headstar” Handhold Suction Unit (Non-sterile)
TW: “華德” 手動式抽吸器(未滅菌)
Risk Class 1
MD

Registration Details

2b06a74b3ee351bcb1c218baddb2b826

Ministry of Health Medical Device Manufacturing No. 007396

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.

I General and plastic surgical devices

I4680 Non-powered, single-patient, portable suction device

Produced in Taiwan, China

Dates and Status

Aug 22, 2018

Aug 22, 2028