DUOMED MEDIUM - Indonesia BPOM Medical Device Registration
DUOMED MEDIUM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902719358. The device is manufactured by MEDI GMBH. & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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MEDI DUOMED
Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDI GMBH. & CO., KG.Country of Origin
Germany
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Nov 01, 2019
Expiry Date
Sep 05, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
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