Taiwan FDA registration 8ef831f919f10d25981fe1167fdb0bd7
Ameri Chlamydomydomiae Test Set (Unsterilized)
TW: 亞美利可披衣菌檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·AMERITEK USA·Registered Aug 02, 2010 – Aug 02, 2020CancelledRegistration details
- Analysis ID
- 8ef831f919f10d25981fe1167fdb0bd7
- Customs Code
- DHA04600100103
Company information
- Manufacturer
- AMERITEK USA
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first grade identification range of Chlamydomydia serological reagent (C.3120) for the management of 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
- Chinese goods;; input
Dates and status
- Registration Date
- Aug 02, 2010
- Expiry Date
- Aug 02, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ameri Chlamydomydomiae Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ef831f919f10d25981fe1167fdb0bd7 and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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