AquaFlexFlow UF500 Plus - Indonesia BPOM Medical Device Registration
AquaFlexFlow UF500 Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420025. The device is manufactured by NUWELLIS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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
NUWELLIS, INC.Country of Origin
United States
Authorized Representative
TRANSMEDIC INDONESIAAR Address
PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137
Registration Date
Jan 15, 2024
Expiry Date
Nov 30, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
SSPC Delivery Catheter
CENTERPOINT SYSTEMS LLC
SANYOU Spinal Rod System (Thoracolumbar) 8
SHANGHAI SANYOU MEDICAL CO., LTD.
SANYOU Spinal Fusion Cage Implant
SHANGHAI SANYOU MEDICAL CO., LTD.
SANYOU Spinal Rod System (Thoracolumbar) 5
SHANGHAI SANYOU MEDICAL CO., LTD.
SANYOU Spinal Rod System (Thoracolumbar) 3
SHANGHAI SANYOU MEDICAL CO., LTD.
SANYOU Spinal Rod System (Thoracolumbar) 4
SHANGHAI SANYOU MEDICAL CO., LTD.
SANYOU Spinal Fusion Cage Instrument
SHANGHAI SANYOU MEDICAL CO., LTD.
MEICEN Thermoplastic Mask 2
GUANGDONG MEICEN MEDICAL EQUIPMENT CO., LTD.
EPIC™ Plus
ST. JUDE MEDICAL BRASIL LTDA
STRYKER Connected OR Hub System
NOVATECH INDUSTRIES