Taiwan FDA registration f4a66ca1a457ef72ee7c54c124dd8a9b

"Sekisui" Trichomonas. V Ag Rapid Test Kit (Non-Sterile)

TW: "績穗" 陰道滴蟲檢測試劑盒 (未滅菌)

Taiwan·Risk Class 1·MD·SEKISUI DIAGNOSTICS, LLC·Registered Jan 09, 2017 – Jan 09, 2027Active

Registration details

Analysis ID: f4a66ca1a457ef72ee7c54c124dd8a9b
License Form: Ministry of Health Medical Device Import No. 017391
Customs Code: DHA09401739103

Company information

Manufacturer: SEKISUI DIAGNOSTICS, LLC
Manufacturer Country: United States
Authorized Representative: ARSENALS IVD CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C2660 Microbial identification and assay equipment
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 09, 2017
Expiry Date: Jan 09, 2027

About this record

Access comprehensive regulatory information for "Sekisui" Trichomonas. V Ag Rapid Test Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4a66ca1a457ef72ee7c54c124dd8a9b and manufactured by SEKISUI DIAGNOSTICS, LLC. The authorized representative in Taiwan is ARSENALS IVD CO., LTD..

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