DS MAREF Intermittent Pneumatic Compression System - Indonesia BPOM Medical Device Registration
DS MAREF Intermittent Pneumatic Compression System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505420037. The device is manufactured by DAESUNG MAREF CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DAESUNG MAREF CO., LTD.Country of Origin
Korea
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Mar 22, 2024
Expiry Date
Dec 18, 2025
Product Type
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