FUJI DRI-CHEM SLIDE Mg - P III - Indonesia BPOM Medical Device Registration
FUJI DRI-CHEM SLIDE Mg - P III is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101811061. 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 FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
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
Aug 28, 2024
Expiry Date
Jun 30, 2028
Product Type
Clinical Chemistry Test System
Magnesium test system (card)
Invitro Diagnostics
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