Taiwan FDA registration 5d47d716f6b6ccf85b14f9c89f81dce1
"LIAISON" Chlamydia trachomatis IgG (Non-Sterile)
TW: "禮雅尚" 砂眼披衣菌IgG檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASORIN IRELAND LTD.·Registered Jun 19, 2017 – Jun 19, 2022ExpiredRegistration details
- Analysis ID
- 5d47d716f6b6ccf85b14f9c89f81dce1
- License Form
- Ministry of Health Medical Device Import No. 017980
- Customs Code
- DHA09401798009
Company information
- Manufacturer
- DIASORIN IRELAND LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of Chlamydomydia serum reagent (C.3120) of medical device management methods.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3120 Chlamydia serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 19, 2017
- Expiry Date
- Jun 19, 2022
About this record
Access comprehensive regulatory information for "LIAISON" Chlamydia trachomatis IgG (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d47d716f6b6ccf85b14f9c89f81dce1 and manufactured by DIASORIN IRELAND LTD.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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