DIESTRO-Trilevel Quality Control Solutions - Indonesia BPOM Medical Device Registration
DIESTRO-Trilevel Quality Control Solutions is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101912216. The device is manufactured by JS MEDICINA ELECTRONICA S.R.L. from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTISERA INDOSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JS MEDICINA ELECTRONICA S.R.L.Country of Origin
Argentina
Authorized Representative
MULTISERA INDOSAAR Address
JL. JEND. SUDIRMAN NO. 689 RT/RW : 21/07
Registration Date
Mar 31, 2023
Expiry Date
Jan 12, 2028
Product Type
Clinical Chemistry Test System
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