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Kaiwood OneStep H. Pylori Fecal Antigen Test (Non-Sterile) - Taiwan Registration 48a3b4b35ad3a2ae3094d22597cb6c41

Access comprehensive regulatory information for Kaiwood OneStep H. Pylori Fecal Antigen Test (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 48a3b4b35ad3a2ae3094d22597cb6c41 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.

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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48a3b4b35ad3a2ae3094d22597cb6c41
Registration Details
Taiwan FDA Registration: 48a3b4b35ad3a2ae3094d22597cb6c41
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Device Details

Kaiwood OneStep H. Pylori Fecal Antigen Test (Non-Sterile)
TW: ้–‹็‰ฉ ็ณžไพฟ่ƒƒๅนฝ้–€่žบๆ—‹ๆกฟ่Œๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

48a3b4b35ad3a2ae3094d22597cb6c41

Ministry of Health Medical Device Import No. 015395

DHA09401539501

Company Information

United States

Product Details

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Jun 30, 2015

Jun 30, 2020

Jan 15, 2020

Cancellation Information

Logged out

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