AirLife ™ Active Humidification System - Indonesia BPOM Medical Device Registration
AirLife ™ Active Humidification System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220991. The device is manufactured by PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. RAVINDRA PUTRAPRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.Country of Origin
Mexico
Authorized Representative
PT. RAVINDRA PUTRAPRATAMAAR Address
Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150
Registration Date
Feb 28, 2023
Expiry Date
Jul 08, 2024
Product Type
Therapeutic Anesthesia Equipment
Anesthesia breathing circuit.
Non Electromedic Non Sterile
AMBU Bluesensor R
AMBU SDN. BHD.
AMBU NEUROLINE 710
AMBU SDN. BHD.
AMBU NEUROLINE Concentric
AMBU SDN. BHD.
PULMODYNE HME Filters
ENGINEERED MEDICAL SYSTEM MALAYSIAN SDN BHD
LIMB-O Single Limb Anesthesia Breathing Circuit
PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.

