QuikRead go iFOBT - Indonesia BPOM Medical Device Registration
QuikRead go iFOBT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206320056. The device is manufactured by AIDIAN LTD from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AIDIAN LTDCountry of Origin
Finland
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Oct 27, 2023
Expiry Date
Dec 31, 2027
Product Type
Manual Hematology Equipment
Occult blood test
Invitro Diagnostics
AIDIAN Uricult
QUIKREAD go CRP Control Low
QuikRead go easy CRP
QUIKREAD go wrCRP
QuikRead go HbA1c Control Set
QuikRead go iFOBT Control Quantitative
QuikRead go CRP Control High
QuikRead go CRP Control
QuikRead Go HbA1c
QuikRead Go Instrument
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