Taiwan FDA registration f6ef7ab6b469acec9ee2e99a38a38021
Xiecke immunoenzyme method Chlamydia IgA antibody reagent
TW: 協克免疫酵素法披衣菌IgA抗體試劑
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Jun 22, 2005 – Jun 22, 2010CancelledRegistration details
- Analysis ID
- f6ef7ab6b469acec9ee2e99a38a38021
- Customs Code
- DHA04400020103
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Enzyme immunoassay was used to detect human serum for IgA antibodies to Chlamydia species.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Jun 22, 2005
- Expiry Date
- Jun 22, 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 Chlamydia IgA 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 f6ef7ab6b469acec9ee2e99a38a38021 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices