MEDIMA Volumetric Infusion Pump - Indonesia BPOM Medical Device Registration
MEDIMA Volumetric Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902023828. The device is manufactured by MEDIMA SP. Z O.O. from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDIMA SP. Z O.O.Country of Origin
Poland
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Jul 13, 2020
Expiry Date
Mar 31, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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