MATRIX Automax 80 - Indonesia BPOM Medical Device Registration
MATRIX Automax 80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209813629. The device is manufactured by TULIP DIAGNOSTICS [P] LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ZEFINDO DARYA MEGATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS [P] LTDCountry of Origin
India
Authorized Representative
ZEFINDO DARYA MEGATAMAAR Address
JL. JEMURSARI 329-331 B
Registration Date
Sep 22, 2023
Expiry Date
May 31, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
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S-BIO Anti B
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S-Bio Anti A,B Monoclonal
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S-BIO Anti D (Rho) (IgM+IgG) Monoclonal
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MATRIX™ Junior CC-0800
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MATRIX ABO/Rho (D) Forward & Reverse Grouping Card with Autocontrol
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