MOSAIQ AiPlex CTD - Indonesia BPOM Medical Device Registration
MOSAIQ AiPlex CTD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420428. The device is manufactured by ALIVEDX SWITZERLAND Ltd from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALIVEDX SWITZERLAND LtdCountry of Origin
Switzerland
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen
Registration Date
Sep 17, 2024
Expiry Date
May 28, 2029
Product Type
Immunological Test System
Multiple autoantibodies immunological test system.
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