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Omega-Imuridep rapid plasma response control group - Taiwan Registration 50ca4ef6c6d5aeeb0cec0dd2bc85ee96

Access comprehensive regulatory information for Omega-Imuridep rapid plasma response control group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50ca4ef6c6d5aeeb0cec0dd2bc85ee96 and manufactured by OMEGA DIAGNOSTICS LTD.. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..

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50ca4ef6c6d5aeeb0cec0dd2bc85ee96
Registration Details
Taiwan FDA Registration: 50ca4ef6c6d5aeeb0cec0dd2bc85ee96
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Device Details

Omega-Imuridep rapid plasma response control group
TW: ๅฅง็ฑณๅŠ -ไพ็น†็ฟ ๆ™ฎๅฟซ้€Ÿ่ก€ๆผฟๅๆ‡‰ๆŽงๅˆถ็ต„
Risk Class 2

Registration Details

50ca4ef6c6d5aeeb0cec0dd2bc85ee96

DHA00601871100

Company Information

United Kingdom

Product Details

Intended for use in combination with IMMUTREP non-treponemal agglutination reagents for qualitative or semi-quantitative analysis of reagin antibodies in serum or plasma.

C Immunology and microbiology

C.3820 Treponema pallidum non-spirochal test

import

Dates and Status

Jan 04, 2008

Jan 04, 2023