MEK Intensive Care Ventilator - Indonesia BPOM Medical Device Registration
MEK Intensive Care Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403310040. The device is manufactured by MEKICS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEKICS CO., LTD.Country of Origin
Korea
Authorized Representative
PT. PERMANA PUTRA MANDIRIAR Address
Jl. Taman Mini Indonesia Indah Pintu 2 atas No.43
Registration Date
May 22, 2024
Expiry Date
Apr 25, 2026
Product Type
Therapeutic Anesthesia Equipment
Continuous ventilator.
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