AQUISEL P-4 System - Indonesia BPOM Medical Device Registration
AQUISEL P-4 System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206819046. The device is manufactured by AQUISEL, S.L. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MIDIF FARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AQUISEL, S.L.Country of Origin
Spain
Authorized Representative
PT. MIDIF FARMAAR Address
Komplek Amarapura Blok E3 No.10 RT.001 Rw.005 Kel.Kademangan Kec.Setu
Registration Date
Jul 11, 2023
Expiry Date
May 25, 2028
Product Type
Manual Hematology Equipment
Erythrocyte sedimentation rate test
Invitro Diagnostics
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TEC 2900-1 MAIN CONSOLE
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TEC 2900-2 Cryo Console
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HISTOLINE TEC 2000 Paraffin Dispenser
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HISTOLINE Automatic Tissue Processor ATP 1000
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HISTO-LINE SD2800 Slide Dryer
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HISTOLINE Manual Rotary Microtome MR2258 And Accessories
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HISTO-LINE WB2800 Water Bath
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