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Nofaferite Human Anti-Chlamydia Enzyme Immunoassay Kit (Unsterilized) - Taiwan Registration c615f7fcc6a7c2088699805241f69d51

Access comprehensive regulatory information for Nofaferite Human Anti-Chlamydia Enzyme Immunoassay Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c615f7fcc6a7c2088699805241f69d51 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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Registration Details
Taiwan FDA Registration: c615f7fcc6a7c2088699805241f69d51
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Device Details

Nofaferite Human Anti-Chlamydia Enzyme Immunoassay Kit (Unsterilized)
TW: ่ซพๆณ•้ตไบบ้กžๆŠ—่‚บ็‚ŽๆŠซ่กฃ่Œ้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c615f7fcc6a7c2088699805241f69d51

DHA04400568307

Company Information

Product Details

It is limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3120 ๆŠซ่กฃ่Œ่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Mar 20, 2007

Mar 20, 2027