Taiwan FDA registration 50ca4ef6c6d5aeeb0cec0dd2bc85ee96

Omega-Imuridep rapid plasma response control group

TW: 奧米加-依繆翠普快速血漿反應控制組

Taiwan·Risk Class 2·OMEGA DIAGNOSTICS LTD.·Registered Jan 04, 2008 – Jan 04, 2023Expired

Registration details

Analysis ID: 50ca4ef6c6d5aeeb0cec0dd2bc85ee96
Customs Code: DHA00601871100

Company information

Manufacturer: OMEGA DIAGNOSTICS LTD.
Manufacturer Country: United Kingdom
Authorized Representative: EUGENE-CHEN CO., LTD.

Product details

Intended Use: Intended for use in combination with IMMUTREP non-treponemal agglutination reagents for qualitative or semi-quantitative analysis of reagin antibodies in serum or plasma.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3820 Treponema pallidum non-spirochal test
Import Information: import

Dates and status

Registration Date: Jan 04, 2008
Expiry Date: Jan 04, 2023

About this record

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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