AQUARIUS Hemofiltration System - Indonesia BPOM Medical Device Registration
AQUARIUS Hemofiltration System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805513596. The device is manufactured by NIKKISO EUROPE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BISAWI GROWS IN HARMONY.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
NIKKISO EUROPE GMBH.Country of Origin
Germany
Authorized Representative
BISAWI GROWS IN HARMONYAR Address
Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat
Registration Date
Dec 16, 2024
Expiry Date
Dec 31, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
Non Radiation Electromedics
AQUARIUS Hemofiltration System
NIKKISO EUROPE GMBH.
ihtDEStiny
IBERHOSPITEX, S.A.
HUNTER Thrombus Extraction Catheter
IBERHOSPITEX, S.A.
HUNTER ST Thrombus Extraction Catheter
IBERHOSPITEX, S.A.
PRYMAX Hemodialysis Catheter Kit
PRYMAX HEALTHCARE LLP
PRYMAX Perfusion - Venous Cannula
PRYMAX HEALTHCARE LLP
FIAB External cardiac stimulator
FIAB S.P.A
MASLANKA Cardiac Grasping Forceps
H. + H. MASLANKA
LSI COR-KNOT MINI Combo Kit
LSI SOLUTIONS INC.
SKINNY PTA Balloon Dilatation Catheter
CNOVATE MEDICAL B.V.