GENTEC Anesthesia Mask - Indonesia BPOM Medical Device Registration
GENTEC Anesthesia Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220306. 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 25, 2022
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Anesthetic gas mask.
Non Electromedic Non Sterile
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