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“Serim” PyloriTek Test Kit(Non-Sterile) - Taiwan Registration 89c89e7bbe69b2e8709c0a640b2bf8c2

Access comprehensive regulatory information for “Serim” PyloriTek Test Kit(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 89c89e7bbe69b2e8709c0a640b2bf8c2 and manufactured by Serim Research Corporation. The authorized representative in Taiwan is TEN QUIN MEDICAL SUPPLY 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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89c89e7bbe69b2e8709c0a640b2bf8c2
Registration Details
Taiwan FDA Registration: 89c89e7bbe69b2e8709c0a640b2bf8c2
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Device Details

“Serim” PyloriTek Test Kit(Non-Sterile)
TW: “偲靈”幽門桿菌測試組(未滅菌)
Risk Class 1
MD

Registration Details

89c89e7bbe69b2e8709c0a640b2bf8c2

Ministry of Health Medical Device Import No. 019784

DHA09401978406

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Nov 06, 2018

Nov 06, 2023