NIPRO Surefuse Plus - Indonesia BPOM Medical Device Registration
NIPRO Surefuse Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902111219. The device is manufactured by NIPRO CORPORATION ODATE FACTORY 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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NIPRO Surefuser Plus
Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO CORPORATION ODATE FACTORYCountry of Origin
Japan
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Sep 12, 2020
Expiry Date
Mar 16, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Electromedic Non Sterile
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