SEKISUI Lp(a) Latex Standard Serum H - Indonesia BPOM Medical Device Registration
SEKISUI Lp(a) Latex Standard Serum H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101125876. The device is manufactured by SEKISUI MEDICAL CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SUMBERMITRA AGUNGJAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEKISUI MEDICAL CO., LTD.Country of Origin
Japan
Authorized Representative
SUMBERMITRA AGUNGJAYAAR Address
Gading Bukit Indah, Blok H/3 Kel Kelapa Gading Barat, Kec Kelapa Gading Jakarta Utara
Registration Date
Sep 20, 2021
Expiry Date
Aug 07, 2025
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
BM Test HbA1c Control (High dan Low)
BM Test HbA1c Diluent
SEKISUI Glycated Albumin Control
SEKISUI Cystatin C Control N
NORUDIA GA
NORUDIA GA Calibrator
SEKISUI Cystatin C Calibrator N
SEKISUI L-FABP Control
NORUDIA L-FABP Calibrator
NORUDIA L- FABP
JOKOH Ref Electrode
JOKOH CO., LTD
THE Electrode
JOKOH CO., LTD
SEKISUI Nanopia CRP
SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT.
JOKOH EX-D Fully Automated Electrolyte Analyzer and Accessories
JOKOH CO., LTD.
JOKOH Standard Solution 1
JOKOH CORPORATION LTD.
JOKOH Standard Solution 2
JOKOH CORPORATION LTD.
SEKISUI Cholestest N Calibrator
SEKISUI MEDICAL CO., LTD.