CARETIUM Reagent Pack - Indonesia BPOM Medical Device Registration
CARETIUM Reagent Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101912988. The device is manufactured by CARETIUM MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAERBA INDOCHEM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARETIUM MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. RAJAERBA INDOCHEMAR Address
GEDUNG PEMBINA GRAHA JL. DI. PANJAITAN NO.45 RAWA BUNGA
Registration Date
Oct 26, 2020
Expiry Date
Jul 29, 2025
Product Type
Clinical Chemistry Test System
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CARETIUM Reagent Pack ABW-4
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CARETIUM Microplate Washer KWP-100 and Accessories
CARETIUM Microplate Reader KC-100 and Accessories
CARETIUM Electrolyte Analyzer K+/Na+/CI- and Accessories
REIGED DIAGNOSTICS Anti-D Monoclonal
GENUINE BIOSYSTEM PVT LMT.
REIGED DIAGNOSTICS Blood Gas, Electrolyte, Metabolite Control
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BIOLAB DIAGNOSTICS Rapid Widal S. Typhi 'O'
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REIGED DIAGNOSTICS Blood Gas Analyzer
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REIGED DIAGNOSTICS Anti-AB Monoclonal
GENUINE BIOSYSTEM PVT LMT.
REIGED DIAGNOSTICS Anti-B Monoclonal
GENUINE BIOSYSTEM PVT LMT.
COMBIWIDAL 'CH' Antigen Slide & Tube Test Method
GENUINE BIOSYSTEM PVT LMT.
REIGED DIAGNOSTICS Anti-A Monoclonal
GENUINE BIOSYSTEM PVT LMT.