VIDAMED Infant Phototherapy - Indonesia BPOM Medical Device Registration
VIDAMED Infant Phototherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220587. 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.
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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
Jun 21, 2022
Expiry Date
Jan 01, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
Non Radiation Electromedics
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VIDAMED Neonatal Incubator
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AIRSEP Oxygen Concentrator
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VIDAMED Neonatal Incubator
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

