HERSILL Perflow 02 - Indonesia BPOM Medical Device Registration
HERSILL Perflow 02 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402817172. The device is manufactured by HERSILL, S.L. from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HERSILL, S.L.Country of Origin
Spain
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Jun 06, 2020
Expiry Date
Apr 06, 2025
Product Type
Monitoring Anesthesia Equipment
Pressure regulator.
Non Electromedic Non Sterile
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