SO 10M - Indonesia BPOM Medical Device Registration
SO 10M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323058. The device is manufactured by DFI CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDISINDO BAHANA.
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DUS 10M
Risk Classification
Product Class
Kelas : 2
Manufacturer
DFI CO., LTD.Country of Origin
Korea
Authorized Representative
MEDISINDO BAHANAAR Address
Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat
Registration Date
May 16, 2023
Expiry Date
Jan 31, 2028
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
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