EXIAS e|1 Cartridge 300 - Indonesia BPOM Medical Device Registration
EXIAS e|1 Cartridge 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101022567. The device is manufactured by EXIAS MEDICAL GMBH from Austria, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EN. RIOCA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EXIAS MEDICAL GMBHCountry of Origin
Austria
Authorized Representative
EN. RIOCA MEDICAAR Address
Komplek Pesona Indah Kapuk Blok A6 Jl. Kapuk Kamal Raya Kav.20A Lantai 3
Registration Date
Jan 27, 2024
Expiry Date
Nov 21, 2028
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
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EXIAS e|1 QC-1 Quality Control Level 1
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EXIAS e|1 Cartridge 300 oQC
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