GENTEC Oxygen Flowmeter Regulator with Humidifier - Indonesia BPOM Medical Device Registration
GENTEC Oxygen Flowmeter Regulator with Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402320103. The device is manufactured by GENTEC (SHANGHAI) CORPORATION from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SANDANA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GENTEC (SHANGHAI) CORPORATIONCountry of Origin
China
Authorized Representative
PT. SANDANAAR Address
JALAN RAYA KEDUNG BARUK NOMOR 25-28
Registration Date
Jul 28, 2023
Expiry Date
Dec 31, 2025
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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