DIASYSTEM Urea (UV) - Indonesia BPOM Medical Device Registration
DIASYSTEM Urea (UV) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101324031. The device is manufactured by DIASYSTEM SCANDINAVIA AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DUAL NOBLE LIGHT.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASYSTEM SCANDINAVIA ABCountry of Origin
Sweden
Authorized Representative
DUAL NOBLE LIGHTAR Address
Ruko Villa Jatibening Toll Blok A no. 2 Jatibening - Bekasi
Registration Date
Oct 04, 2023
Expiry Date
May 25, 2027
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
Invitro Diagnostics
DIASYSTEM Bilirubin (Total)
DIASYSTEM Album (BCG)
DIASYSTEM Bilirubin (Direct)
DIASYSTEM Creatinine Jaffe
DIASYSTEM Uric Acid (TBHBA)
DIASYSTEM Unilab N
DIASYSTEM Cholesterol (Total)
DIASYSTEM Glucose (GOD)
DIASYSTEM CDT240 Auto Chemistry Analyzer and Accesories
GIESSE Hematology Analyzer Lyse 2 GS5
GIESSE DIAGNOSTICS.
I-SENS i-Smart Electrolyte Quality Control (Ca2+)
I-SENS
I-SMART QC Blood Gas Electrolyte Metabolite Quality Control Multi Level
I-SENS, INC.
DIASYSTEM Bilirubin (Total)
DIASYSTEM SCANDINAVIA AB
DIASYSTEM Creatinine Jaffe
DIASYSTEM SCANDINAVIA AB
DIASYSTEM Uric Acid (TBHBA)
DIASYSTEM SCANDINAVIA AB
Giesse_Hematology Analyzer Diluent GS3
GIESSE DIAGNOSTICS.