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Formosa One Sure Micro-albumin Rapid Test Kit(Non-Sterile) - Taiwan Registration 750de1402ecc5f82efa4d47904dc54c4

Access comprehensive regulatory information for Formosa One Sure Micro-albumin Rapid 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 750de1402ecc5f82efa4d47904dc54c4 and manufactured by Formosa Biomedical Technology Co., Ltd. Yilan Factory. The authorized representative in Taiwan is FORMOSA BIOMEDICAL TECHNOLOGY CORPORATION.

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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750de1402ecc5f82efa4d47904dc54c4
Registration Details
Taiwan FDA Registration: 750de1402ecc5f82efa4d47904dc54c4
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Device Details

Formosa One Sure Micro-albumin Rapid Test Kit(Non-Sterile)
TW: ๅฐๅก‘็”Ÿ้†ซ่ฟ…็Ÿฅๅฐฟ็™ฝ่›‹็™ฝๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

750de1402ecc5f82efa4d47904dc54c4

Ministry of Health Medical Device Manufacturing No. 007780

Company Information

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)".

A Clinical chemistry and clinical toxicology

A1645 Urine protein or albumin (non-quantitative) test system

Produced in Taiwan, China

Dates and Status

May 29, 2019

May 29, 2024