DP Fusion VP1 Infusion Pump - Indonesia BPOM Medical Device Registration
DP Fusion VP1 Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127509. 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 PT. 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
PT. INDOPRIMA BIONETAR Address
Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150
Registration Date
Dec 01, 2021
Expiry Date
Jan 01, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
INFINIUM ADS II Anesthesia Delivery System
INFINIUM MEDICAL, INC.
INFINIUM OMNI II Patient Monitor
INFINIUM MEDICAL INC.
INFINIUM OMNI VIEW Central Station
INFINIUM MEDICAL INC.
INFINIUM Patient Monitor
INFINIUM MEDICAL INC.
CARDIOLINE XR450R
RUNNER S.R.L
ANCOOL Ultrasonic Pulmonary Function Testing
ANCOOL TECHNOLOGY CO., LTD
EF Medica Stress Test Electrodes FS 50 LG
EF MEDICA S.R.L
HITEC Closed Suction Catheter 24h
HITEC MEDICAL CO., LTD
DPMMED DPFusion VP1 Infusion Pump
CHANGSA DEEPMED MEDICAL TECHNOLOGY CO.,LTD
HITEC Closed Suction Catheter 72h
HITEC MEDICAL CO., LTD