Taiwan FDA registration a36c0bfb642fcdcd01f19ab5c3680e31

LANNER Immunoglobulin E Reagent Kit/IgE

TW: 朕江免疫球蛋白E試劑套組

Taiwan·Risk Class 2·MD·LANNER BIOTECHNOLOGY CO., LTD.·Registered Jul 17, 2018 – Jul 17, 2028Active

Registration details

Analysis ID: a36c0bfb642fcdcd01f19ab5c3680e31
License Form: Ministry of Health Medical Device Manufacturing No. 005988

Company information

Manufacturer: LANNER BIOTECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LANNER BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: It is used for in vitro quantitative analysis of immunoglobulin E content in human serum or EDTA and heparin plasma, suitable for Hitachi 7170 automatic biochemistry analyzer.
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C5510 Immunoglobulins A, G, M, D and E Immunoassay System
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jul 17, 2018
Expiry Date: Jul 17, 2028

About this record

Access comprehensive regulatory information for LANNER Immunoglobulin E Reagent Kit/IgE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a36c0bfb642fcdcd01f19ab5c3680e31 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..

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