VERIFY U500 Urine Analyzer - Indonesia BPOM Medical Device Registration
VERIFY U500 Urine Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102320449. The device is manufactured by ACON BIOTECH (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EXXEL MAIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACON BIOTECH (HANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
PT. EXXEL MAINAR Address
JALAN RAJAWALI SELATAN.RUKO MULTI GUNA KEMAYORAN BLOK.6N.JAKARTA UTARA
Registration Date
Mar 13, 2023
Expiry Date
Aug 10, 2027
Product Type
Clinical Laboratory Equipment
Automated urinalysis system.
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