GENESIS Anaesthesia Machine - Indonesia BPOM Medical Device Registration
GENESIS Anaesthesia Machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403613005. The device is manufactured by HERSILL S.L. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDIARTA MARTA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HERSILL S.L.Country of Origin
Spain
Authorized Representative
PT. ANDIARTA MARTA UTAMAAR Address
Pusat Niaga Duta Mas Blok C2 No. 11-12 Jl. RS Fatmawati 39
Registration Date
Dec 07, 2020
Expiry Date
Aug 27, 2025
Product Type
Therapeutic Anesthesia Equipment
Anesthetic vaporizer.
Non Radiation Electromedics
