Xpert Xpress SARS-CoV-2/Flu/RSV - Indonesia BPOM Medical Device Registration
Xpert Xpress SARS-CoV-2/Flu/RSV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303122051. The device is manufactured by CEPHEID from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDQUEST JAYA GLOBAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CEPHEIDCountry of Origin
United States
Authorized Representative
MEDQUEST JAYA GLOBALAR Address
Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A
Registration Date
Apr 08, 2022
Expiry Date
Dec 31, 2024
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics
Xpert Xpress CoV-2 Flu RSV Plus
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XPERT BCR-ABL Ultra
Xpert Check
XPERT MTB/RIF Ultra
Xpert MRSA NxG
Xpert MTB/XDR
XPERT Xpress SARS-COV-2
Xpert BCR-ABL Ultra
DIAGAST QWALYS INSTRUMENT
DIAGAST
ECHOSENS Fibroscan 430 Mini
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Procleix UltrioPlex E Positive Calibrators
GRIFOLS DIAGNOSTIC SOLUTIONS INC
XPERT HPV Assay Kit
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Xpert HIV-1 Qual XC
CEPHEID AB
Procleix UltrioPlex E Assay Rehearsors Kit
GRIFOLS DIAGNOSTIC SOLUTIONS INC.
Xpert Carba-R
CEPHEID AB
Scinomed Plasma Collection Machine
SCINOMED (SHANGHAI) BIO-TECH CO., LTD
XPERT MRSA NxG
CEPHEID AB
Xpert Xpress SARS-CoV-2
CEPHEID AB

