Taiwan FDA registration c615f7fcc6a7c2088699805241f69d51

Nofaferite Human Anti-Chlamydia Enzyme Immunoassay Kit (Unsterilized)

TW: 諾法鐵人類抗肺炎披衣菌酵素免疫分析套組 (未滅菌)

Taiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered Mar 20, 2007 – Mar 20, 2027Active

Registration details

Analysis ID: c615f7fcc6a7c2088699805241f69d51
Customs Code: DHA04400568307

Company information

Manufacturer: GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH
Manufacturer Country: Germany
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) 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: Mar 20, 2007
Expiry Date: Mar 20, 2027

About this record

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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