GENTEC Flowmeter Humidifier - Indonesia BPOM Medical Device Registration
GENTEC Flowmeter Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402320107. 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 SANDANA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GENTEC (SHANGHAI) CORPORATIONCountry of Origin
China
Authorized Representative
SANDANAAR Address
JALAN RAYA KEDUNG BARUK NOMOR 25-28
Registration Date
Aug 01, 2023
Expiry Date
Dec 31, 2025
Product Type
Monitoring Anesthesia Equipment
Compensated thorpe tube flowmeter.
Non Electromedic Non Sterile
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