MEK Photo Therapy Device - Indonesia BPOM Medical Device Registration
MEK Photo Therapy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902310042. The device is manufactured by MEKICS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. 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
Taman Mini Pintu II Atas No.9 Jakarta Timur
Registration Date
Oct 07, 2019
Expiry Date
May 15, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
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