ADVIA 360/560 Diluent (Dil) - Indonesia BPOM Medical Device Registration
ADVIA 360/560 Diluent (Dil) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220084. The device is manufactured by DIATRON MI PLC from Hungary, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIATRON MI PLCCountry of Origin
Hungary
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Apr 28, 2022
Expiry Date
Mar 04, 2025
Product Type
Hematological Reagents
Blood cell diluents
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