VIASURE CMV q Real Time PCR Detection Kit - Indonesia BPOM Medical Device Registration
VIASURE CMV q Real Time PCR Detection Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321332. The device is manufactured by CERTEST BIOTEC S.L. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is STANDARD BIOSENSOR INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CERTEST BIOTEC S.L.Country of Origin
Spain
Authorized Representative
STANDARD BIOSENSOR INDONESIAAR Address
L'AVENUE BUILDING UNIT C, LT. 21, JL. RAYA PASAR MINGGU KAV. 16
Registration Date
May 30, 2024
Expiry Date
Feb 01, 2026
Product Type
Serological Reagents
Cytomegalovirus serological reagents.
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STANDARD F TnI FIA
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STANDARD F iFOB FIA
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STANDARD F TnI/CK-MB Combo FIA
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STANDARD F NT-proBNP FIA
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STANDARD F CK-MB FIA
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STANDARD F D-dimer FIA
SD BIOSENSOR HEALTHCARE PVT. LTD.

