FLEXICARE VeoFlo High Flow Nasal Cannula - Indonesia BPOM Medical Device Registration
FLEXICARE VeoFlo High Flow Nasal Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403813661. The device is manufactured by FLEXICARE MEDICAL (DONGGUAN) LIMITED. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINABAKTI NIAGAPERKASA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FLEXICARE MEDICAL (DONGGUAN) LIMITED.Country of Origin
China
Authorized Representative
PT. BINABAKTI NIAGAPERKASAAR Address
Jl. Kebon Jeruk I No. 32 Taman Sari Jakarta Barat
Registration Date
Jul 18, 2022
Expiry Date
Jan 21, 2025
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Non Sterile
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