CAPTURE-R READY SCREEN (3) - Indonesia BPOM Medical Device Registration
CAPTURE-R READY SCREEN (3) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209512566. The device is manufactured by IMMUCOR INC. 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
IMMUCOR INC.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
Feb 25, 2024
Expiry Date
Jul 14, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
Invitro Diagnostics
IMMUCOR Anti-IgG,-C3d; Polyspecific (Murine Monoclonal) (Green or Uncolored) Gamma Clone
IMMUCOR Anti-S (Monoclonal) Gamma-clone
IMMUCOR Gamma EGA Kit
IMMUCOR Weak D Cells
RESt (Rabbit Erythrocyte Stroma for Adsorption of Cold Agglutinins Anti-I , Anti-H or Anti-IH)
IMMUCOR Complement Control Cells
Gamma ELU-KIT II
IMMUCOR Reagent Red Blood Cells CAPTURE-R Ready-Screen (I and II)
PANOSCREEN I, II and III
IMMUCOR Anti-H Lectin
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