GENTEC Coaxial Breathing Circuit - Indonesia BPOM Medical Device Registration
GENTEC Coaxial Breathing Circuit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220157. 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. MEDISTRON ENERGY.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GENTEC (SHANGHAI) CORPORATIONCountry of Origin
China
Authorized Representative
PT. MEDISTRON ENERGYAR Address
Ruko Cinere Terrace Commercial Blok JC No. 5, Jl. Telaga Warna
Registration Date
May 21, 2022
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Anesthesia breathing circuit.
Non Electromedic Non Sterile
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