Taiwan FDA registration f7b8d497cd1d7cb821316a7131a37d47

"Ruicheng" Bairka Chlamydomydomia pneumoniae IgM screening reagent (unsterilized)

TW: "銳誠" 拜爾卡肺炎披衣菌IgM篩檢試劑 (未滅菌)

Taiwan·Risk Class 1·Labsystems Diagnostics Oy·Registered Feb 07, 2013 – Feb 07, 2028Active

Registration details

Analysis ID: f7b8d497cd1d7cb821316a7131a37d47
Customs Code: DHA04401268808

Company information

Manufacturer: Labsystems Diagnostics Oy
Manufacturer Country: Finland
Authorized Representative: RAFA INTERNATIONAL CORP.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3120 披衣菌血清試劑
Import Information: import

Dates and status

Registration Date: Feb 07, 2013
Expiry Date: Feb 07, 2028

About this record

Access comprehensive regulatory information for "Ruicheng" Bairka Chlamydomydomia pneumoniae IgM screening reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7b8d497cd1d7cb821316a7131a37d47 and manufactured by Labsystems Diagnostics Oy. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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