Taiwan FDA registration ae811dfd5ef9509676712ca629bf0d94
Xiec fluorescence method Chlamydomydia IgA serum antibody reagent
TW: 協克螢光法披衣菌 IgA 血清抗體試劑
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Apr 18, 2005 – Apr 18, 2010CancelledRegistration details
- Analysis ID
- ae811dfd5ef9509676712ca629bf0d94
- Customs Code
- DHA04400002700
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- 用於血清試驗中鑑定對血清中披衣菌(C.pneumoniae, C.trachomatis, C.psittaci)IgA抗體.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Apr 18, 2005
- Expiry Date
- Apr 18, 2010
- Cancellation Date
- Nov 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Xiec fluorescence method Chlamydomydia IgA serum antibody reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae811dfd5ef9509676712ca629bf0d94 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
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