Taiwan FDA registration c6a51435040b6f67d2c09cdee1b7478f
Xiecke immunoenzyme method Chlamydomydia IgG antibody reagent
TW: 協克免疫酵素法披衣菌IgG抗體試劑
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Oct 13, 2005 – Oct 13, 2010CancelledRegistration details
- Analysis ID
- c6a51435040b6f67d2c09cdee1b7478f
- Customs Code
- DHA04400093700
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- It is used in serum tests to identify antibodies to Chlamydia spp. in serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Oct 13, 2005
- Expiry Date
- Oct 13, 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 Xiecke immunoenzyme method Chlamydomydia IgG 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 c6a51435040b6f67d2c09cdee1b7478f and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
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