AIR LIQUIDE Suction Pump - Indonesia BPOM Medical Device Registration
AIR LIQUIDE Suction Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603211359. The device is manufactured by AIR LIQUIDE MEDICAL SYSTEMS S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ESA MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AIR LIQUIDE MEDICAL SYSTEMS S.P.A.Country of Origin
Italy
Authorized Representative
PT. ESA MEDIKA MANDIRIAR Address
ESA 8 Building, 10th Floor, Jl. Ir. Soekarno Kavling 3-5
Registration Date
Sep 17, 2020
Expiry Date
Apr 30, 2024
Product Type
Surgical Equipment
Powered suction pump.
Non Radiation Electromedics
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