FREKA Tube FR 12, 120 cm, ENFit - Indonesia BPOM Medical Device Registration
FREKA Tube FR 12, 120 cm, ENFit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805127346. The device is manufactured by CLINICO MEDICAL SP. Z O.O. from Poland, 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
CLINICO MEDICAL SP. Z O.O.Country of Origin
Poland
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 13, 2023
Expiry Date
Apr 26, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
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