VIDAMED Neonatal Incubator - Indonesia BPOM Medical Device Registration
VIDAMED Neonatal Incubator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221147. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARIMIA JAYA MANDIRI.
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
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTDCountry of Origin
China
Authorized Representative
PT. ARIMIA JAYA MANDIRIAR Address
Gedung Konica lantai 3A Jl. Gunung Sahari Raya nomor 78
Registration Date
Oct 24, 2022
Expiry Date
Dec 31, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal incubator.
Non Radiation Electromedics
VIDAMED Patient Monitor
SERENITY Anesthesia Machine
NESCO Neonatal Monitor
BOZTRON Defibrillator Monitor
VIDAMED Infusion Pump
VIDAMED Syringe Pump
VIDAMED Infant Radiant Warmer
VIDAMED Neonatal Ventilator
VIDAMED Infant Phototherapy
COMEN Temperature Control System
AIRSEP Oxygen Concentrator
CAIRE MEDICAL TECHNOLOGY (CHENGDU) CO., LTD.
CAIRE Oxygen Concentrator
CAIRE MEDICAL TECHNOLOGY (CHENGDU) CO., LTD.
AIRSEP Oxygen Concentrator
CAIRO INC.
VIDAMED Infant Phototherapy
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Defibrillator Monitor
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Defibrillator Monitor
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD
VIDAMED Neonatal Incubator
SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD

