GESAN Urea UV LR - Indonesia BPOM Medical Device Registration
GESAN Urea UV LR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101717622. The device is manufactured by GESAN PRODUCTION S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GRAHA MEGATAMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GESAN PRODUCTION S.R.L.Country of Origin
Italy
Authorized Representative
PT. GRAHA MEGATAMA INDONESIAAR Address
RUKO MAHKOTA ANCOL BLOK. E 39 JL. BUDI MULIA KEL. PADEMANGAN BARAT
Registration Date
Mar 03, 2021
Expiry Date
Feb 18, 2025
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
Invitro Diagnostics
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