HEMOSIL Fibrinogen-C - Indonesia BPOM Medical Device Registration
HEMOSIL Fibrinogen-C is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207712927. The device is manufactured by INSTRUMENTATION LABORATORY COMPANY. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INSTRUMENTATION LABORATORY COMPANY.Country of Origin
United States
Authorized Representative
PT. ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Jul 11, 2024
Expiry Date
Dec 31, 2027
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
HEMOSIL Apixaban Calibrators
HEMOSIL Rivaroxaban Controls
HEMOSIL Apixaban Controls
HEMOSIL Rivaroxaban Calibrators
HEMOSIL Protein S Activity
HEMOSIL La Positive Control
HEMOSIL La Negative Control
HEMOSIL Rinse Solution
HEMOSIL Protein C
HEMOSIL Factor IX Deficient Plasma
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