DP Fusion SP1 Syringe Pump - Indonesia BPOM Medical Device Registration
DP Fusion SP1 Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902323076. The device is manufactured by CHANGSA DEEPMED MEDICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOPRIMA BIONET.
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
CHANGSA DEEPMED MEDICAL TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
Dec 27, 2023
Expiry Date
Jun 25, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
INFINIUM OMNI Patient Monitor
INFINIUM MEDICAL INC.
DP Fusion SP1S Syringe Pump
CHANGSA DEEPMED MEDICAL TECHNOLOGY CO.,LTD
EF Medica ECG Electrodes W 50 SG
EF MEDICA S.R.L
EF Medica ECG Electrodes RT-24
EF MEDICA S.R.L
EF Medica ECG Electrode F-30SG
EF MEDICA S.R.L
EF Medica ECG Electrodes F 3741 SG
EF MEDICA S.R.L
OSYPKA Medical ICON Non Invasive Cardiac
OSYPKA MEDICAL GMBH.
AESCULON Non Invasive Cardiac Output Electrical Cardiometry
OSYPKA MEDICAL GMBH.
Cardioline XR600
CARDIOLINE S.P.A.
ICON CORE Electrical Cardiometry
OSYPKA MEDICAL GMBH.