Taiwan FDA registration c595644cb138af506ae3158fd4f8b34a
"Artron" Chlamydia trachomatis Test Kit (Non-Sterile)
TW: "艾壯" 披衣菌快速檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered May 11, 2018 – May 11, 2023ExpiredRegistration details
- Analysis ID
- c595644cb138af506ae3158fd4f8b34a
- License Form
- Ministry of Health Medical Device Import No. 019041
- Customs Code
- DHA09401904102
Company information
- Manufacturer
- ARTRON LABORATORIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- Medley Limited
Product details
- Intended Use
- Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3120 Chlamydia serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 11, 2018
- Expiry Date
- May 11, 2023
About this record
Access comprehensive regulatory information for "Artron" Chlamydia trachomatis 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 c595644cb138af506ae3158fd4f8b34a and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is Medley Limited.
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