NIPROCART A2F 760 - Indonesia BPOM Medical Device Registration
NIPROCART A2F 760 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805612680. The device is manufactured by NIPRO RENAL SOLUTION SPAIN, S.L.U., from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO RENAL SOLUTION SPAIN, S.L.U.,Country of Origin
Spain
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Aug 26, 2024
Expiry Date
Nov 28, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Non Sterile
RENAL - Sol A1
RENAL LABORATORIES SDN., BHD.
RENAL-SOL A23
RENAL LABORATORIES SDN.,BHD.
RENAL - Sol B1
RENAL LABORATORIES SDN.,BHD
HD Integra DR-1 Automatic Dialyzer Reprocessor System
JKS BIOMEDICAL SDN. BHD.
SUREFLUX-G Hemodialyzer
NIPRO CORPORATION ODATE FACTORY
SUREFLUX-Eโข Hemodialyzer
NIPRO CORPORATION ODATE FACTORY
SUREFLUX-Lโข Hemodialyzer
NIPRO CORPORATION ODATE FACTORY
SUREFLUX- N Triacetat Hollow Dialyzer
NIPRO CORPORATION ODATE FACTORY
ELISIOโข-L Synthetic Hollow Fiber Polynephron
NIPRO CORPORATION ODATE FACTORY
GUIDEPLUS II Guide Extension Catheter
NIPRO CORPORATION ODATE FACTORY

