FiCA – I FIA Analyzer - Indonesia BPOM Medical Device Registration
FiCA – I FIA Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420105. The device is manufactured by SURE BIO-TECH (USA) CO., LTD from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOLAB ARTHA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SURE BIO-TECH (USA) CO., LTDCountry of Origin
United States
Authorized Representative
PT. INDOLAB ARTHA MEDIKAAR Address
Komp Ruko Sunter Paradise Tahap II Blok.A4 No.43. Sunter Agung Podomoro
Registration Date
Nov 06, 2024
Expiry Date
Jan 31, 2029
Product Type
Immunology Laboratory Equipment and Reagents
Immunofluorometer equipment. (Electrically Operated)
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