MPM Nasal Oxygen Cannula - Indonesia BPOM Medical Device Registration
MPM Nasal Oxygen Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403916008. The device is manufactured by HANGZHOU SUPERDS INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HANGZHOU SUPERDS INDUSTRY CO., LTD.Country of Origin
China
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Jan 23, 2022
Expiry Date
Dec 12, 2024
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Sterile
MPM Nasal Oxygen Cannula
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