Taiwan FDA registration d2c1620c43a04b76a617bbe278586d39
"Sekisui" Bacterial Vaginosis Test (Non-Sterile)
TW: "績穗" 細菌性陰道炎檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·GRYPHUS DIAGNOSTICS, LLC·Registered Mar 06, 2017 – Mar 06, 2022ExpiredRegistration details
- Analysis ID
- d2c1620c43a04b76a617bbe278586d39
- License Form
- Ministry of Health Medical Device Import No. 017559
- Customs Code
- DHA09401755902
Company information
- Manufacturer
- GRYPHUS 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
- Mar 06, 2017
- Expiry Date
- Mar 06, 2022
About this record
Access comprehensive regulatory information for "Sekisui" Bacterial Vaginosis Test (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 d2c1620c43a04b76a617bbe278586d39 and manufactured by GRYPHUS DIAGNOSTICS, LLC. The authorized representative in Taiwan is ARSENALS IVD CO., LTD..
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