DIRUI BF- FBH Lyse - Indonesia BPOM Medical Device Registration
DIRUI BF- FBH Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208023148. The device is manufactured by DIRUI INDUSTRIAL., CO, LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FAITHFUL MEDICAL GRACE.
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
DIRUI INDUSTRIAL., CO, LTDCountry of Origin
China
Authorized Representative
FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Nov 03, 2023
Expiry Date
Jul 01, 2028
Product Type
Hematological Reagents
Red cell lysing reagent.
Invitro Diagnostics
DIRUI Probe Cleanser I
DIRUI BF-5D DILUENT
DIRUI BCC-3900 Automatic Hematology Analyzer and Accessories
DIRUI BF-FDT IN LYSE
DIRUI BCC- 3D Diluent
DIRUI Probe Cleanser
ROLES THAT
DIRUI CLEANSER BCC-3000 PROBE CLEANSER
DIRUI BF-CRP REAGENT KIT
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