MPM Silicone Manual Resuscitator Set - Indonesia BPOM Medical Device Registration
MPM Silicone Manual Resuscitator Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403704398. The device is manufactured by BESMED HEALTH BUSINESS CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BESMED HEALTH BUSINESS CORP.Country of Origin
Taiwan (China)
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Dec 13, 2021
Expiry Date
May 24, 2024
Product Type
Therapeutic Anesthesia Equipment
Manual emergency ventilator.
Non Electromedic Sterile
MPM Silicone Manual Resuscitator Set (with hand strap)
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