Spinreact Uric Acid-LQ - Indonesia BPOM Medical Device Registration
Spinreact Uric Acid-LQ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421205. The device is manufactured by SPINREACT, S.A.U from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SEIMITSU DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPINREACT, S.A.UCountry of Origin
Spain
Authorized Representative
SEIMITSU DIAGNOSTICSAR Address
Harton Tower 7th Floor, Jl. Boulevard Artha Gading, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara.
Registration Date
Jun 25, 2024
Expiry Date
Dec 31, 2027
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
Invitro Diagnostics
