FUJI DRI-CHEM SLIDE ALP-PIII - Indonesia BPOM Medical Device Registration
FUJI DRI-CHEM SLIDE ALP-PIII is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101717440. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION MINAMIASHIGARA NAKANUMA OFFICE from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
PT. FUJIFILM INDONESIAAR Address
: EightyEight@Kasablanka Office Tower A, Lantai 36 Jl. Casablanca Raya Kav. 88, Desa/Kelurahan Menteng Dalam, Kec. Tebet, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12870 No Telp: 021-21282182
Registration Date
Apr 30, 2024
Expiry Date
Jun 30, 2028
Product Type
Clinical Chemistry Test System
Alkaline phosphatase or isoenzymes test system (card)
Invitro Diagnostics
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