ALINITY c Ultra HDL Reagent Kit - Indonesia BPOM Medical Device Registration
ALINITY c Ultra HDL Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124383. The device is manufactured by SEKISUI DIAGNOSTICS P.E.I, INC from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEKISUI DIAGNOSTICS P.E.I, INCCountry of Origin
Canada
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
Wisma Pondok Indah 2, Suite 1000, Jl. Sultan Iskandar Muda Kav V - TA
Registration Date
Jul 08, 2024
Expiry Date
Apr 29, 2029
Product Type
Clinical Chemistry Test System
Lipoprotein test system (kit & cair)
Invitro Diagnostics
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