Conox QM7000-M GB2 - Indonesia BPOM Medical Device Registration
Conox QM7000-M GB2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402024716. The device is manufactured by FRESENIUS VIAL S.A.S from France, 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
FRESENIUS VIAL S.A.SCountry of Origin
France
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
Aug 21, 2020
Expiry Date
Aug 31, 2024
Product Type
Monitoring Anesthesia Equipment
Electrical peripheral nerve stimulator.
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