Taiwan FDA registration 71e4b8dd0019bdf2065f2512885acd8c
IgA antibody reagent for Chlamydomydomiae pneumonia
TW: 協克披衣菌肺炎IgA抗體試劑
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered May 30, 2005 – May 30, 2010CancelledRegistration details
- Analysis ID
- 71e4b8dd0019bdf2065f2512885acd8c
- Customs Code
- DHA04400010800
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Enzyme immunoassay was used to sexually test human serum for IgA antibody to Chlamydae pneumoniae.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- May 30, 2005
- Expiry Date
- May 30, 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 IgA antibody reagent for Chlamydomydomiae pneumonia in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 71e4b8dd0019bdf2065f2512885acd8c 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