MDX Hemaline 300 Diluent - Indonesia BPOM Medical Device Registration
MDX Hemaline 300 Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320432. The device is manufactured by URIT MEDICAL ELECTRONIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERMAN MEDTEK DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
URIT MEDICAL ELECTRONIC CO., LTD.Country of Origin
China
Authorized Representative
HERMAN MEDTEK DIAGNOSTICSAR Address
Jl. Lingkar Luar Barat, Puri Kembangan, Komplek Rukan Puri Mansion Blok A No.16 Kel.Kembangan Selatan Kec.Kembangan, Kota Jakarta Barat, DKI Jakarta
Registration Date
Feb 13, 2023
Expiry Date
Dec 31, 2025
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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