Spinreact Spintrol P - Indonesia BPOM Medical Device Registration
Spinreact Spintrol P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421117. 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 PT. SEIMITSU DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPINREACT, S.A.UCountry of Origin
Spain
Authorized Representative
PT. SEIMITSU DIAGNOSTICSAR Address
Harton Tower 7th Floor, Jl. Boulevard Artha Gading, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara.
Registration Date
Jun 10, 2024
Expiry Date
Dec 31, 2027
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
Spinreact Cholesterol
Spinreact ALP - LQ
Spinreact Triglycerides - LQ
SPINREACT Total Proteins
Spinreact Uric Acid-LQ
SPINREACT Albumin
SPINREACT Glucose
SPINREACT Bilirubin Total
SPINREACT UREA UV
SPINREACT Spintrol Calibrator
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