Taiwan FDA registration 5c75ec868cda1dcf9ce87555733b355a
Leica Novocastra Liquid Mouse Monoclonal Antibody Estrogen Receptor
TW: 錸卡諾摩凱斯特雌激素受體小鼠單株抗體試劑
Registration details
- Analysis ID
- 5c75ec868cda1dcf9ce87555733b355a
- License Form
- Ministry of Health Medical Device Import No. 032018
- Customs Code
- DHA05603201800
Company information
- Manufacturer
- LEICA BIOSYSTEMS NEWCASTLE LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is used for in vitro diagnostics, by light microscopy, qualitative analysis of estrogen receptor antigens in paraffin sections of breast tissue.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1860 Immunopathological histochemical reagents and kits
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 09, 2019
- Expiry Date
- Jan 09, 2029
About this record
Access comprehensive regulatory information for Leica Novocastra Liquid Mouse Monoclonal Antibody Estrogen Receptor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c75ec868cda1dcf9ce87555733b355a and manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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