FOYOMED Silicone Manual Resuscitator - Indonesia BPOM Medical Device Registration
FOYOMED Silicone Manual Resuscitator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321593. The device is manufactured by XIAMEN COMPOWER MEDICAL TECH. CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDISTRON ENERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
XIAMEN COMPOWER MEDICAL TECH. CO., LTD.Country of Origin
China
Authorized Representative
PT. MEDISTRON ENERGYAR Address
Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna
Registration Date
Sep 15, 2023
Expiry Date
Jul 05, 2026
Product Type
Therapeutic Anesthesia Equipment
Manual emergency ventilator.
Non Electromedic Non Sterile
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