GOOD AIR - Indonesia BPOM Medical Device Registration
GOOD AIR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703020040. The device is manufactured by Bien Air Surgery Ltd from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. OPMIC PERKASA MANDIRI.
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BIEN AIR
Risk Classification
Product Class
Kelas : 2
Manufacturer
Bien Air Surgery LtdCountry of Origin
Switzerland
Authorized Representative
PT. OPMIC PERKASA MANDIRIAR Address
Jl.Puri Kencana Blok K7-3D 3rd Fl Kembangan Jakarta 11610
Registration Date
Dec 20, 2024
Expiry Date
Dec 31, 2027
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat electric or pneumatic surgical drill.
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