NIPRO Syringe Pump SMARTFUSION - Indonesia BPOM Medical Device Registration
NIPRO Syringe Pump SMARTFUSION is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902021373. The device is manufactured by DAIKEN MEDICAL CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAIKEN MEDICAL CO., LTD.Country of Origin
Japan
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Mar 23, 2020
Expiry Date
Oct 28, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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