Taiwan FDA registration 0323168158e1a3c02e1a26e3b06576ba
"Leica" Bond Ready-to-Use Primary Antibody S-100 (Polyclonal)(Non-Sterile)
TW: “錸卡”邦德即用型S100一級抗體(多株抗體) (未滅菌)
Registration details
- Analysis ID
- 0323168158e1a3c02e1a26e3b06576ba
- License Form
- Ministry of Health Medical Device Import No. 019872
- Customs Code
- DHA09401987203
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
- Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
- 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
- Dec 03, 2018
- Expiry Date
- Dec 03, 2028
About this record
Access comprehensive regulatory information for "Leica" Bond Ready-to-Use Primary Antibody S-100 (Polyclonal)(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 0323168158e1a3c02e1a26e3b06576ba and manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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