ARUMALAB LD LYSE ON 580 - Indonesia BPOM Medical Device Registration
ARUMALAB LD LYSE ON 580 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420281. The device is manufactured by GENRUI BIOTECH INC from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELBA LAB MEDIKA.
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ARUMALAB LD LYSE AR 580
Risk Classification
Product Class
Kelas : 2
Manufacturer
GENRUI BIOTECH INCCountry of Origin
China
Authorized Representative
PT. ELBA LAB MEDIKAAR Address
GRAHA BUMI INDAH LANTAI II ROOM 2005, JL. RAYA KALIMALANG KAV. AGRARIA NO. 8-0 RT/RW 002/016 KEL. DUREN SAWIT KEC. DUREN SAWIT JAKARTA TIMUR
Registration Date
Sep 27, 2024
Expiry Date
Sep 24, 2027
Product Type
Hematological Reagents
Red cell lysing reagent.
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