SUREFLUX-E™ Hemodialyzer - Indonesia BPOM Medical Device Registration
SUREFLUX-E™ Hemodialyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805022272. The device is manufactured by NIPRO CORPORATION ODATE FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
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SUREFLUX™-E Hemodialyzer
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
Nov 18, 2024
Expiry Date
Oct 02, 2029
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile
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