DreamStation Go Humidifier - Indonesia BPOM Medical Device Registration
DreamStation Go Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403023842. The device is manufactured by RESPIRONICS INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RESPIRONICS INC.Country of Origin
United States
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2
Registration Date
Jul 13, 2020
Expiry Date
Jan 13, 2025
Product Type
Therapeutic Anesthesia Equipment
Respiratory gas humidifier.
Non Radiation Electromedics
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