VIDAS® TB-IGRA (TBRA) - Indonesia BPOM Medical Device Registration
VIDAS® TB-IGRA (TBRA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220345. The device is manufactured by BIOMERIEUX S.A. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOMERIEUX S.A.Country of Origin
France
Authorized Representative
ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Aug 01, 2024
Expiry Date
Dec 31, 2028
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
Invitro Diagnostics
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VIDAS® IFNg QC PANEL (IFNg QC)
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ID Color Catalase ( ID - ASE )
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BIOMERIEUX Oxidase Reagent
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VITEK 2 AST-N425
BIOMERIEUX INC.
B.R.A.H.M.S PCT LIVES
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ELVASENSE Blood Glucose Test Strip
TAIDOC TECHNOLOGY CORPORATION
BIOMERIEUX Serum Free
BIOMERIEUX S.A.
Eppendorf Centrifuge 5425R
EPPENDORF SE, GERMANY
VIDAS HBs Ag Ultra Confirmation
BIOMERIEUX SA.