ICARE Pulse Oximeter - Indonesia BPOM Medical Device Registration
ICARE Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502320853. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL ENERGY ALKESINDO.
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
GUANGDONG BIOLIGHT MEDITECH CO., LTD.Country of Origin
China
Authorized Representative
PT. GLOBAL ENERGY ALKESINDOAR Address
GLOBAL ENERGY ALKESINDO
Registration Date
Oct 18, 2023
Expiry Date
Oct 16, 2026
Product Type
Monitoring Cardiology Equipment
Oximeter.
Non Radiation Electromedics
BIOLIGHT Central Monitoring System
BIOLIGHT Multi Parameter Patient Monitor
BLT Patient Monitor
ICARE Digital Electrocardiograph
ICARE Digital Electrocardiograph
ICARE Multi Parameter Patient Monitor
ICARE Multi Parameter Patient Monitor
ICARE Pulse Oximeter
ICARE Pulse Oximeter
ICARE Digital Electrocardiograph
MEDIKIT SUPERCATH ZTU-V
TOGO MEDIKIT CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD.
AUTOCHECK Ultrasound System
ACO HEALTHCARE CO., LTD
EUNICEMED Back Support TL
COMFORT PLUS CORPORATION
EUNICEMED Knee Support 11" AG+
COMFORT PLUS CORPORATION

