XN-L CHECK™ L2 - Indonesia BPOM Medical Device Registration
XN-L CHECK™ L2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208612300. The device is manufactured by DASH, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DASH, INC.Country of Origin
United States
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Aug 01, 2023
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
ClearLLab Control Cells Normal
ClearLLab Control Cells Abnormal
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