NIPRO Arterial Venous Fistula Needles - Indonesia BPOM Medical Device Registration
NIPRO Arterial Venous Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805122026. The device is manufactured by NIPRO (THAILAND) CORPORATION LIMITED from Thailand, 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 (THAILAND) CORPORATION LIMITEDCountry of Origin
Thailand
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Apr 12, 2021
Expiry Date
Nov 30, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
NIPRO Insulin Disposable Syringe With Needle 1 ml
BAXTER AV Fistula Needles
VACUETTE Blood Collection Set + Luer Adapter
VACUETTE Safety Blood Collection Set + Luer Adapter
VACUETTE SAFETY Blood Collection Sets
NIPRO Sterile Syringe for Single Use Without Needle DOSESAVER LD 1ml
DIACAN Buttonhole
DIACAN Safety
DIACAN PRO Fistula Needle
NIPRO Hypodermic Needle
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-E™ Hemodialyzer
NIPRO CORPORATION ODATE FACTORY
SUREFLUX-L™ Hemodialyzer
NIPRO CORPORATION ODATE FACTORY
SUREFLUX- N Triacetat Hollow Dialyzer
NIPRO CORPORATION ODATE FACTORY
ELISIO™-L Synthetic Hollow Fiber Polynephron
NIPRO CORPORATION ODATE FACTORY
NIPROCART A2F 760
NIPRO RENAL SOLUTION SPAIN, S.L.U.,