GESAN Direct Bilirubin LR - Indonesia BPOM Medical Device Registration
GESAN Direct Bilirubin LR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101915797. The device is manufactured by GESAN PRODUCTION SRL 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 SRLCountry 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 08, 2021
Expiry Date
Feb 20, 2025
Product Type
Clinical Chemistry Test System
Bilirubin (total or direct) test system (kit & cair)
Invitro Diagnostics
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