PRESS 2 - Indonesia BPOM Medical Device Registration
PRESS 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203020740. The device is manufactured by OPTIKON 2000 SPA from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OPMIC PERKASA MANDIRI.
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PULSAR 2
Risk Classification
Product Class
Kelas : 2
Manufacturer
OPTIKON 2000 SPACountry of Origin
Italy
Authorized Representative
PT. OPMIC PERKASA MANDIRIAR Address
Jl.Puri Kencana Blok K7-3D 3rd Fl Kembangan Jakarta 11610
Registration Date
Mar 06, 2020
Expiry Date
Sep 24, 2024
Product Type
Surgical Eye Equipment
Phacofragmentation system.
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