SIEMENS N FLC Control SL2 - Indonesia BPOM Medical Device Registration
SIEMENS N FLC Control SL2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220405. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH.Country of Origin
Germany
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Sep 19, 2022
Expiry Date
Feb 16, 2025
Product Type
Immunological Test System
Immunoglobulin (light chain specific) immunological test system.
Invitro Diagnostics
N Antiserum Human Albumin
SIEMENS N Latex Lp(a) Reagent
SIEMENS N Latex Beta 2–Microglobulin
SIEMENS HEALTHINEERS N Protein Standard SL
SIEMENS N FLC Standard SL
SIEMENS N Latex sTfR
SIEMENS N Reaction Buffer
SIEMENS N Antiserum to Human IgG
SIEMENS N FLC Supplementary Reagent
SIEMENS N/T Protein Control SL/M
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