HEMOSIL von Willebrand Factor Activity - Indonesia BPOM Medical Device Registration
HEMOSIL von Willebrand Factor Activity is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320259. The device is manufactured by INSTRUMENTATION LABORATORY COMPANY from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ENSEVAL MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INSTRUMENTATION LABORATORY COMPANYCountry of Origin
United States
Authorized Representative
ENSEVAL MEDIKA PRIMAAR Address
JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG
Registration Date
Jul 03, 2024
Expiry Date
Dec 31, 2027
Product Type
Haematology Package and Kit
Factor deficiency test.
Invitro Diagnostics
HEMOSIL von Willebrand Factor Antigen
GEM System Evaluator Lvl 3
HEMOSIL Silica Clotting Time
GEM Hematocrit Evaluator 2
GEM System Evaluator Lvl 2
GEM Hematocrit Evaluator 3
GEM Hematocrit Evaluator 1
ELVASENSE Mini Safety Lancet
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