iQ Calibrator - Indonesia BPOM Medical Device Registration
iQ Calibrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123532. The device is manufactured by BECKMAN COULTER, INC. from United States, and is classified as Risk Class Kelas Resiko : B. 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
BECKMAN COULTER, INC.Country of Origin
United States
Authorized Representative
DHH TRADING INDONESIAAR Address
Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan
Registration Date
Nov 28, 2024
Expiry Date
Mar 28, 2029
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
FlowClean Cleaning Agent
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