Taiwan FDA registration fa00668317d80e3c40da2448dcff7949
"Puse" Chlamydia Enzyme Immunoassay Assay Kit (Unsterilized)
TW: "普生" 披衣菌酵素免疫檢驗分析套組 (未滅菌)
Taiwan·Risk Class 1·GENERAL BIOLOGICALS CORP.·Registered Jun 04, 2014 – Jun 04, 2024ExpiredRegistration details
- Analysis ID
- fa00668317d80e3c40da2448dcff7949
Company information
- Manufacturer
- GENERAL BIOLOGICALS CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- Domestic
Dates and status
- Registration Date
- Jun 04, 2014
- Expiry Date
- Jun 04, 2024
About this record
Access comprehensive regulatory information for "Puse" Chlamydia Enzyme Immunoassay Assay 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 fa00668317d80e3c40da2448dcff7949 and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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