DUMO FA MICROPIPETTE - Indonesia BPOM Medical Device Registration
DUMO FA MICROPIPETTE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102126189. The device is manufactured by ACCUMAX LAB DEVICES PVT LTD. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DUMO DIAGNOSTICS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ACCUMAX LAB DEVICES PVT LTD.Country of Origin
India
Authorized Representative
PT. DUMO DIAGNOSTICS INDONESIAAR Address
JL. KALIBATA SELATAN II NO 2 RT 002/04 KEL. KALIBATA, KEC. PANCORAN, JAKARTA SELATAN
Registration Date
Oct 19, 2021
Expiry Date
May 28, 2024
Product Type
Clinical Laboratory Equipment
Pipetting and diluting system for clinical use.
Invitro Diagnostics
DUMOLABS Salmonella Paratyphi BO
DIALAB G.M.B.H
DUMOLABS Creatinine, Mod. Jaffe
DIALAB G.M.B.H
DUMO VARIABLE MICROPIPETTE
ACCUMAX LAB DEVICES PVT LTD
DUMOLABS Uric Acid TBHBA, Enzymatic, Colorimetric
DIALAB G.M.B.H
DUMOLABS Auto Chemistry Analyzer DC150W
SHENZHEN HETO MEDICAL TECH CO., LTD
DUMOLABS DC20 Semi-Auto Chemistry Analyzer
GENRUI BIOTECH INC
DUMOLABS Urea UV Auto, GLDH
DIALAB G.M.B.H.
DUMOLABS GPT (ALT), mod. IFCC
DIALAB G.M.B.H
DUMOLABS Salmonella Paratyphi CO
DIALAB G.M.B.H
DUMOLABS Salmonella Paratyphi AO
DIALAB G.M.B.H

