DUMOLABS Urea UV Auto, GLDH - Indonesia BPOM Medical Device Registration
DUMOLABS Urea UV Auto, GLDH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123669. The device is manufactured by DIALAB G.M.B.H. from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DUMO DIAGNOSTICS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIALAB G.M.B.H.Country of Origin
Austria
Authorized Representative
PT. DUMO DIAGNOSTICS INDONESIAAR Address
JL. KALIBATA SELATAN II NO 2 RT 002/04 KEL. KALIBATA, KEC. PANCORAN, JAKARTA SELATAN
Registration Date
Jun 23, 2021
Expiry Date
Dec 31, 2023
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
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