DNlite-DKD uPTM-FetA ELISA Kit - Indonesia BPOM Medical Device Registration
DNlite-DKD uPTM-FetA ELISA Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420889. The device is manufactured by BIO PREVENTIVE MEDICINE CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIO PREVENTIVE MEDICINE CORP.Country of Origin
Taiwan (China)
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Dec 02, 2024
Expiry Date
Feb 15, 2029
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
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