m-PIMA ™ Analyser - Indonesia BPOM Medical Device Registration
m-PIMA ™ Analyser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304220128. The device is manufactured by PLEXUS MANUFACTURING SDN. BHD from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ALERE HEALTH.
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m-PIMA ™ Analyser
Risk Classification
Product Class
Kelas : 2
Manufacturer
PLEXUS MANUFACTURING SDN. BHDCountry of Origin
Malaysia
Authorized Representative
ALERE HEALTHAR Address
K-Link Tower Lantai 18 Zona D, E, dan F Jl. Gatot Subroto Kav. 59 A RT 001 RW 003 Kel. Kuningan Timur, Kec. Setiabudi, Jakarta Selatan
Registration Date
Dec 09, 2022
Expiry Date
Jun 04, 2027
Product Type
Immunology Laboratory Equipment and Reagents
RNA Preanalytical Systems.
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