AMBIX INTROCATH - Indonesia BPOM Medical Device Registration
AMBIX INTROCATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902916443. The device is manufactured by PHS MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FRESENIUS KABI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PHS MEDICAL GMBHCountry of Origin
Germany
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
Oct 07, 2019
Expiry Date
Mar 08, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Percutaneous, implanted, long-term intravascular catheter.
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