BECKMAN COULTER D-Dimer Control - Indonesia BPOM Medical Device Registration
BECKMAN COULTER D-Dimer Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207220175. The device is manufactured by LSI MEDIENCE CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DHH TRADING INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
LSI MEDIENCE CORPORATIONCountry of Origin
Japan
Authorized Representative
DHH TRADING INDONESIAAR Address
Gedung World Trade Center 3, Lt. 20, Jl. Jend. Sudirman Kav. 29-31, Kel. Karet, Kec. Setiabudi, Jakarta Selatan, DKI Jakarta
Registration Date
Nov 18, 2022
Expiry Date
Feb 10, 2026
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
iQ Calibrator
BECKMAN COULTER, INC.
Iris Diluent Pack
BECKMAN COULTER INC.
BECKMAN COULTER DxU 810c Iris Urine Chemistry Analyzer
BECKMAN COULTER, INC
INFINITY Lithium Reagent for Beckman Coulter AU Chemistry Analyzers
FISHER DIAGNOSTICS
G6PD Control Intermediate
SENTINEL CH. S.P.A
G6PD Control Normal
SENTINEL CH. S.P.A
COULTER TruColor Wright Stain Buffer
POLYSCIENCES INC.
COULTER TruColor Wright Stain
POLYSCIENCES INC.
Access HIV combo V2 QC
BIO-RAD
BECKMAN COULTER Digoxin
MICROGENICS CORPORATION

