CONOX Sensor - Indonesia BPOM Medical Device Registration
CONOX Sensor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001320131. The device is manufactured by FRESENIUS KABI (NANCHANG) CO., LTD. from China, 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 KABI (NANCHANG) CO., LTD.Country of Origin
China
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
Jul 18, 2023
Expiry Date
Sep 16, 2027
Product Type
Diagnostic Neurology Equipment
Cutaneous electrode.
Non Electromedic Non Sterile
CONOX Pediatric Sensor
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Infusion SET VL ST 02
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INJECTOMAT Lines
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CONOX Pediatric Sensor
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