ALINITY c Direct LDL Reagent Kit - Indonesia BPOM Medical Device Registration
ALINITY c Direct LDL Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101814954. 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. INC.Country 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
Mar 13, 2023
Expiry Date
Jan 12, 2028
Product Type
Clinical Chemistry Test System
Lipoprotein test system (kit & cair)
Invitro Diagnostics
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