GENTEC Suction Regulators - Indonesia BPOM Medical Device Registration
GENTEC Suction Regulators is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903421124. The device is manufactured by GENTEC (SHANGHAI) CORPORATION from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SANDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GENTEC (SHANGHAI) CORPORATIONCountry of Origin
China
Authorized Representative
PT. SANDANAAR Address
Jl. Raya Kedung Baruk No. 25-28
Registration Date
Nov 20, 2024
Expiry Date
Dec 31, 2025
Product Type
General Hospital Equipment and Other Individuals
Vacuum-powered body fluid suction apparatus
Non Electromedic Non Sterile
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