ARUMAMED LD LYSE 5-DIFF - Indonesia BPOM Medical Device Registration
ARUMAMED LD LYSE 5-DIFF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420295. 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. ARDIKHA UMRAN ABADI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GENRUI BIOTECH INCCountry of Origin
China
Authorized Representative
PT. ARDIKHA UMRAN ABADIAR Address
Jl. Bintara VIII No.100A RT 006 RW 003
Registration Date
Oct 07, 2024
Expiry Date
Oct 03, 2027
Product Type
Hematological Reagents
Red cell lysing reagent.
Invitro Diagnostics
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ARUMAMED LH LYSE 5-DIFF
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ARUMAMED DILUENT 5-DIFF
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ARUMAMED Hematology Control Set 5 Diff
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ARUMAMED Hematology Control Normal 5 Diff
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ARUMAMED Hematology Control Normal 3 Diff
PENRUI BIOTECH INC.