Taiwan FDA registration 891083434128ab3666ca95bd7526c9f0

"Kipfu" Chlamydom pneumoniae nucleic acid test panel (not extinguished)

TW: "基普復" 肺炎披衣菌核酸檢驗試劑組(未滅菌)

Taiwan·Risk Class 1·GeneProof a. s.·Registered Oct 25, 2023 – Oct 25, 2028Active

Registration details

Analysis ID: 891083434128ab3666ca95bd7526c9f0
Customs Code: DHA09402328809

Company information

Manufacturer: GeneProof a. s.
Manufacturer Country: Czechia
Authorized Representative: MEDTRI CO., LTD.

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: Input;; QMS/QSD

Dates and status

Registration Date: Oct 25, 2023
Expiry Date: Oct 25, 2028

About this record

Access comprehensive regulatory information for "Kipfu" Chlamydom pneumoniae nucleic acid test panel (not extinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 891083434128ab3666ca95bd7526c9f0 and manufactured by GeneProof a. s.. The authorized representative in Taiwan is MEDTRI CO., LTD..

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