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EASEmed Carcinoma embryonic Antigen (CEA) Rapid Test Kit - Taiwan Registration ef40236cfaee1bd0b300c075777b8082

Access comprehensive regulatory information for EASEmed Carcinoma embryonic Antigen (CEA) Rapid Test Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ef40236cfaee1bd0b300c075777b8082 and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. 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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ef40236cfaee1bd0b300c075777b8082
Registration Details
Taiwan FDA Registration: ef40236cfaee1bd0b300c075777b8082
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Device Details

EASEmed Carcinoma embryonic Antigen (CEA) Rapid Test Kit
TW: ้†ซ่ฉฆ็พŽ็™Œ่ƒš่ƒŽๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

ef40236cfaee1bd0b300c075777b8082

Ministry of Health Medical Device Manufacturing No. 004434

Company Information

Taiwan, Province of China

Product Details

This product is a qualitative detection of carcinoembryonic antigen in human serum.

C Immunology and microbiology devices

C6010 Tumor-associated antigen immunoassay system

Produced in Taiwan, China

Dates and Status

Jan 13, 2014

Jan 13, 2029