Q-Smart - Indonesia BPOM Medical Device Registration
Q-Smart is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102320681. The device is manufactured by BIOSCITEC GMBH, from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEGMED DISTRIBUTION INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSCITEC GMBH,Country of Origin
Germany
Authorized Representative
PT. SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Nov 06, 2023
Expiry Date
Oct 26, 2026
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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