FRESENIUS CompoDock - Indonesia BPOM Medical Device Registration
FRESENIUS CompoDock is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209705600. The device is manufactured by SANMINA-SCI. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SANMINA-SCI.Country of Origin
Sweden
Authorized Representative
PT. FRESENIUS KABI INDONESIAAR Address
Menara Bidakara 1 Lt.19, Jl. Gatot Subroto Kav 71 - 73 Menteng Dalam, Tebet, Jakarta Selatan 12870
Registration Date
Mar 13, 2021
Expiry Date
Jan 18, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Transfer set.
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